Syneos Health

Senior CRA - Phase I oncology trials - Hamburg/Berlin region

Syneos Health · Full Time · 3 hours ago

Syneos Health

🌎 Germany ⭐ 5-10 yrs exp 💼 Others

The Senior CRA will perform on-site and remote monitoring visits to ensure regulatory, ICH-GCP, and protocol compliance for Phase I oncology trials. They are responsible for site management, source data verification, and escalating serious issues to the project team to ensure data integrity and patient safety.

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Director, Safety and PV Systems (Innovation & AI)

Syneos Health · Full Time · 18 hours ago

Syneos Health

🌎 Serbia ⭐ 10+ yrs exp 💼 Software Development

The Director will own the roadmap and delivery of end-to-end safety and pharmacovigilance technology solutions, including AI/ML prototypes and automation. They will lead cross-functional teams and innovation councils to scale proven patterns and ensure regulatory compliance.

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Medical Writer II (Project/Program Coordinator)

Syneos Health · Full Time · 18 hours ago

Syneos Health

🌎 India ⭐ 2-5 yrs exp 💼 Product

The Medical Writer II manages end-to-end scientific writing workflows, including publication planning, journal submissions, and congress activity coordination. They ensure accurate documentation and adherence to regulatory standards while providing operational support to cross-functional teams.

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Medical Writer II (MLR Reviewer)

Syneos Health · Full Time · 18 hours ago

Syneos Health

🌎 India ⭐ 2-5 yrs exp 💼 Writing

The Medical Writer II performs end-to-end scientific writing, including managing publication plans and ensuring documents are MLR-ready for submission. They also mentor less experienced writers and collaborate across departments to ensure document accuracy and regulatory compliance.

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Medical Writer II (Veeva Vault Technician)

Syneos Health · Full Time · a day ago

Syneos Health

🌎 India ⭐ 2-5 yrs exp 💼 Writing

The Medical Writer II manages end-to-end scientific writing workflows, including publication planning and Veeva Vault document management. They also mentor less experienced writers and ensure all deliverables meet regulatory and client standards.

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Statistical Programmer II

Syneos Health · Full Time · a day ago

Syneos Health

🌎 India ⭐ 2-5 yrs exp 💼 Software Development

The Statistical Programmer II will collaborate with cross-functional teams to deliver clinical solutions and support drug development processes. They are responsible for applying technical expertise to meet customer needs and contribute to the successful execution of clinical studies.

agile organization compliance

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Senior CRA in Oncology Phase I - Sponsor dedicated - Home Based in Paris Area

Syneos Health · Full Time · a day ago

Syneos Health

🌎 France ⭐ 5-10 yrs exp 💼 Others

The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.

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Sr Statistical Programmer(ADaM & TLF)

Syneos Health · Full Time · a day ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Software Development

The Senior Statistical Programmer develops custom programming code for summary tables, listings, and graphs while ensuring quality standards and regulatory compliance. They also act as a lead programmer, directing activities for other personnel and participating in sponsor meetings.

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Local Clinical Trial Manager - Single Sponsor

Syneos Health · Full Time · a day ago

Syneos Health

🌎 Germany ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol, GCP, and regulatory compliance. They also manage study-specific risks, oversee clinical team deliverables, and coordinate with functional leaders to meet study milestones.

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Sr CRA for FSP BU based in South Korea

Syneos Health · Full Time · a day ago

Syneos Health

🌎 South Korea ⭐ 5-10 yrs exp 💼 Others

The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.

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(Sr.) Site Contract Specialist, Philippines

Syneos Health · Full Time · a day ago

Syneos Health

🌎 Philippines ⭐ 5-10 yrs exp 💼 Legal

The Site Contract Specialist manages the end-to-end contract process, including drafting, negotiating, and executing clinical trial agreements and budgets. They also collaborate with internal and external stakeholders to ensure compliance with project timelines and regulatory standards.

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(Sr.) Site Contract Specialist, Malaysia

Syneos Health · Full Time · a day ago

Syneos Health

🌎 Malaysia ⭐ 5-10 yrs exp 💼 Legal

Administers contract management processes including the negotiation and preparation of clinical trial agreements, budgets, and related documents. Collaborates with internal and external stakeholders to ensure compliance with timelines, quality standards, and regulatory requirements.

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Sr. Site Contracts Lead

Syneos Health · Full Time · 3 days ago

Syneos Health

🌎 Spain 💵 $67700 - $115K per year ⭐ 5-10 yrs exp 💼 Others

The Sr. Site Contracts Lead oversees the negotiation of clinical study agreements and investigator budgets while serving as a subject matter expert for global site contracting issues. They also manage internal and sponsor stakeholder expectations, provide training to team members, and ensure contractual strategies align with overall study start-up plans.

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Project Financial Analyst II

Syneos Health · Full Time · 4 days ago

Syneos Health

🌎 United Kingdom ⭐ 2-5 yrs exp 💼 Finance

The Project Financial Analyst II is responsible for preparing, reconciling, and analyzing business unit revenue, contracts, and project metrics. They support the Business Unit Controller by drafting financial forecasts, variance analyses, and ensuring accurate reporting within established timelines.

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CRA II or Sr CRA assigned to client (FSP) - Bogotá, Barranquilla, Medellín - Colombia Home-Based

Syneos Health · Full Time · 4 days ago

Syneos Health

🌎 Colombia ⭐ 2-5 yrs exp 💼 Others

The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the study lifecycle.

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Principal Medical Writer - Publications

Syneos Health · Full Time · 4 days ago

Syneos Health

🌎 United States 💵 $80600 - $175K per year ⭐ 10+ yrs exp 💼 Writing

The Principal Medical Writer leads the development of complex clinical documents and manages medical writing activities across various studies. They also provide expert peer reviews, mentor junior staff, and ensure all deliverables meet regulatory and client standards.

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Sr Statistcal Programmer

Syneos Health · Full Time · 4 days ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Software Development

The Senior Statistical Programmer develops custom code to generate summary tables, listings, and graphs while ensuring quality standards and regulatory compliance. They also act as a lead programmer, directing project activities and mentoring junior personnel.

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Sr CRA-Beijing

Syneos Health · Full Time · 4 days ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Others

The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and provide guidance to site staff to meet project objectives.

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Tijdelijke CRA positie in Nederland

Syneos Health · Full Time · 4 days ago

Syneos Health

🌎 Netherlands ⭐ 2-5 yrs exp 💼 Others

The Clinical Research Associate (CRA) will perform site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They are responsible for managing site activities, verifying clinical data accuracy, and maintaining essential study documentation.

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Senior/Principal Medical Editor – FSP (Regulatory Documents)

Syneos Health · Full Time · 4 days ago

Syneos Health

🌎 United States 💵 $62000 - $175K per year ⭐ 5-10 yrs exp 💼 Legal

The role involves maintaining regulatory compliance for medical documents and representing the editorial group within study teams. It also includes managing project timelines, mentoring staff, and performing quality reviews to ensure adherence to industry standards.

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Senior/Principal Medical Editor - FSP

Syneos Health · Full Time · 4 days ago

Syneos Health

🌎 United Kingdom ⭐ 5-10 yrs exp 💼 Writing

The role involves copyediting and performing quality reviews on complex medical documents to ensure compliance with regulatory standards. Additionally, the editor will lead project deliverables, mentor staff, and provide technical expertise to cross-departmental study teams.

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Project Specialist - RBM focus (Spnsor-dedicated)

Syneos Health · Full Time · 5 days ago

Syneos Health

🌎 Hungary, Poland, Serbia, Turkey, Ukraine ⭐ 2-5 yrs exp 💼 Product

The Project Specialist will execute risk-based monitoring strategies and analyze clinical data to identify trends and potential risks. They will also collaborate with study teams to implement corrective actions and ensure regulatory compliance and patient safety.

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Senior Clinical Data Associate (Rave)

Syneos Health · Full Time · 5 days ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Healthcare

This role involves leading clinical data associates in data management activities and providing support for global clinical trials. Responsibilities include performing UAT, managing data discrepancies, overseeing study builds, and mentoring junior staff.

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Clinical Scientist - Oncology

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Scientist collaborates with the Medical Director to develop medical plans and perform rigorous medical data reviews to identify risks and trends. They serve as the primary interface between internal teams and customers to ensure project milestones and quality deliverables are met.

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Sponsor Dedicated CRAI/CRA II Regionalized North Italy - Home Based Milan area

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Italy 💵 €36000 - €53000 per year ⭐ 0-2 yrs exp 💼 Others

The CRA will perform site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They will also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.

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Senior CRA - FSP - KSA Based

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Saudi Arabia ⭐ 5-10 yrs exp 💼 Others

The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying clinical data accuracy, managing investigational product inventory, and maintaining essential study documentation.

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Regulatory Consultant (CMC-EU, GCC & AU)

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Legal

The consultant will independently manage regulatory submissions, including gap analyses and technical documentation for global regulatory agencies. They will also act as a subject matter expert on multidisciplinary project teams to support product life cycle development and client interactions.

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Senior Regulatory Associate (CMC - EU,APAC, gulf countries.)

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Legal

The Senior Regulatory Associate prepares and submits IND, marketing, and lifecycle maintenance applications while ensuring compliance with government regulations. They also conduct quality control reviews, manage project-specific activities, and provide mentorship to team members.

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Global Study Manager

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Canada ⭐ 5-10 yrs exp 💼 Others

The Global Study Manager will collaborate with cross-functional teams to deliver clinical solutions and drive customer success across the drug development continuum. They are responsible for managing complex study requirements while maintaining an agile mindset to meet project goals.

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CRA I. Valencia. Sponsor dedicated.

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Spain ⭐ 0-2 yrs exp 💼 Others

The CRA I performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.

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Country - Study Operations Manager

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Canada ⭐ 5-10 yrs exp 💼 Others

The Study Operations Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol and regulatory compliance. They coordinate with functional leaders to meet study milestones, manage risks, and oversee the performance of clinical team members.

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Country Study Operations Manager

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Canada ⭐ 5-10 yrs exp 💼 Others

The Country Study Operations Manager oversees site management, clinical monitoring, and regulatory compliance to ensure patient safety and data integrity. They are responsible for managing study budgets, identifying operational risks, and coordinating with cross-functional teams to meet study milestones.

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Data Scientist_ Remote in Bulgaria

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Bulgaria ⭐ 5-10 yrs exp 💼 Others

The role involves merging and standardizing datasets from multiple sources while performing data profiling and quality analysis. You will also develop predictive models, optimize algorithms, and communicate data-driven insights to stakeholders.

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CRA I

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Italy ⭐ 0-2 yrs exp 💼 Others

The CRA I performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential trial documentation.

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Project manager - Medical Writing

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Germany ⭐ 5-10 yrs exp 💼 Product

The project manager oversees medical writing deliverables, manages cross-functional teams, and ensures high-quality work products. They also supervise staff, handle performance reviews, and support business development activities such as proposal and budget preparation.

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CRA II - Shanghai

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Manage project components, write monitoring reports, and collaborate with cross-functional teams to support clinical trial operations.

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CRA I/II - Beijing

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the project lifecycle.

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Clinical Data Reviewer - Oncology

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 United States 💵 $80600 - $145K per year ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Data Reviewer performs specialized clinical review of large, multi-faceted data sets to ensure readiness for milestones like interim analysis and study closeout. They identify data inconsistencies, generate queries, and monitor for safety signals while collaborating with the broader study team.

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Sr Medical Writer - Late Phase - Inflammation

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Spain 💵 $70100 - $145K per year ⭐ 5-10 yrs exp 💼 Writing

The Senior Medical Writer leads the preparation of complex clinical documents while ensuring scientific accuracy and adherence to regulatory standards. They coordinate cross-functional activities, mentor junior staff, and manage client relationships to ensure deliverables are completed on time and within budget.

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Sr Director, Epidemiology RWE

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Canada ⭐ 10+ yrs exp 💼 Others

The Senior Director serves as the lead scientific resource for Real-World Evidence (RWE) projects, providing executive oversight and driving business development opportunities. They are responsible for guiding scientific strategy, managing project delivery, and fostering relationships with sponsors and thought leaders.

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Sr Medical Writer - Late Phase Inflammation

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Writing

Leads the preparation and completion of complex medical writing deliverables, ensuring scientific accuracy and adherence to regulatory standards. Coordinates cross-functional activities and mentors less experienced writers while managing client relationships and project timelines.

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Principal Research Scientist ONC -Clinical Development Scientist (Sponsor Dedicated/ Remote US)

Syneos Health · Full Time · 7 days ago

Syneos Health

🌎 United States 💵 $79800 - $139K per year ⭐ 5-10 yrs exp 💼 Healthcare

The Principal Research Scientist is responsible for developing, validating, and optimizing bioanalytical methods while coordinating laboratory activities. They also supervise and mentor scientific staff to ensure compliance with corporate policies and operational objectives.

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RTSM/eCOA Manager

Syneos Health · Full Time · 7 days ago

Syneos Health

🌎 Spain 💵 $95000 - $175K per year ⭐ 5-10 yrs exp 💼 Others

The manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory standards while managing project budgets and timelines. They act as the primary liaison between the company and the customer to facilitate successful study launch, conduct, and closeout.

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Site Contracts Specialist II/ Sr SCS - Poland, Multiple Sponsors

Syneos Health · Full Time · 7 days ago

Syneos Health

🌎 Poland ⭐ 5-10 yrs exp 💼 Others

The role involves managing the end-to-end contract process for clinical trials, including drafting, negotiating, and executing site agreements and budgets. Additionally, the specialist will mentor junior staff and collaborate with internal and external stakeholders to ensure project timelines and quality standards are met.

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CRA II - Multi Sponsor

Syneos Health · Full Time · 7 days ago

Syneos Health

🌎 United Kingdom ⭐ 2-5 yrs exp 💼 Others

The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level communication, verify clinical data accuracy, and support subject safety and data integrity throughout the study lifecycle.

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CRA II - Beijing

Syneos Health · Full Time · 7 days ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

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Clinical Trial Manager II

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 Brazil ⭐ 5-10 yrs exp 💼 Healthcare

Responsible for overseeing site management, clinical monitoring, and data integrity to ensure patient safety and regulatory compliance. Collaborates with functional leaders to manage study milestones, risk mitigations, and the development of clinical study tools.

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Clinical Project Manager (Early Phase)

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 Spain 💵 $80600 - $210K per year ⭐ 5-10 yrs exp 💼 Product

The role involves managing Trial Master File (TMF) plans, coordinating study deliverables across functional departments, and overseeing vendor performance. Additionally, the manager handles financial reporting, budget reconciliation, and risk mitigation strategies to ensure study milestones are met.

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Principal Statistical Programmer (European Timezone Only)

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 Armenia, Belgium, France, Germany, Greece, Hungary, Ireland, Netherlands, Poland, Portugal, Serbia, South Africa, Spain, United Kingdom ⭐ 10+ yrs exp 💼 Software Development

Lead the development of custom programming code to generate summary tables, listings, and graphs as specified in statistical analysis plans. Direct programming activities, monitor deliverables, and mentor junior programmers to ensure data accuracy and integrity.

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Sponsor Dedicated CRA II/Sr CRA I - Home Based ITA

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 Italy 💵 €40000 - €62000 per year ⭐ 2-5 yrs exp 💼 Others

The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also includes managing site-level activities, verifying clinical data integrity, and overseeing investigational product reconciliation.

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Medical Information. FSP. Barcelona or Madrid.

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Healthcare

The role involves elaborating scientific answers and bibliographic dossiers based on reference documents for external distribution. It also requires generating metrics, analyzing request trends, and leveraging AI tools to improve the efficiency of medical information activities.

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Clin Ops Specialist

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 South Korea ⭐ 0-2 yrs exp 💼 Others

The specialist supports clinical monitoring staff with site management and ensures compliance with protocol requirements and guidelines. They are also responsible for maintaining the Trial Master File, tracking regulatory documents, and coordinating site supplies.

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Sr CRA I - Guangzhou

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory requirements. Develop quality monitoring tools and collaborate with cross-functional teams to support clinical trial operations.

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Site Contracts Specialist II or Senior - Sponsor dedicated - Home Based France

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 France ⭐ 5-10 yrs exp 💼 Others

The role involves administering contract management processes and negotiating budgets and agreements for industry-sponsored clinical trials. It also requires coordinating with legal and clinical operations teams to ensure the accurate execution and archival of Clinical Trial Agreements.

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Project Manager / Clinical Trial Lead - sponsor dedicated - Germany

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 Germany ⭐ 5-10 yrs exp 💼 Product

The role involves leading and managing global clinical trials to ensure quality execution, compliance with GCP, and adherence to budgets and timelines. The Project Manager acts as the primary liaison between the company and the customer while overseeing interdisciplinary research studies.

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Principal Clinical Trial Regulatory Affairs

Syneos Health · Full Time · 10 days ago

Syneos Health

🌎 Poland ⭐ 10+ yrs exp 💼 Legal

Acts as a Regulatory Subject Matter Expert to lead site activation pathways and manage clinical trial application dossiers. Responsible for strategic client relationship management, regulatory impact assessments, and overseeing the submission of core documents.

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Sr Director, Epidemiology RWE assigned to client

Syneos Health · Full Time · 10 days ago

Syneos Health

🌎 Colombia ⭐ 10+ yrs exp 💼 Others

Provides scientific oversight and expertise for Real-World Life Sciences (RWLP) projects, including the development of protocols and study reports. Leads business development efforts through project proposals and bid defenses while maintaining relationships with sponsors and clinical investigators.

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Clinical Research Associate II/ Sr CRA I, Denmark - Sponsor-dedicated

Syneos Health · Full Time · 11 days ago

Syneos Health

🌎 Denmark ⭐ 2-5 yrs exp 💼 Healthcare

The role involves performing site qualification, initiation, and monitoring visits to ensure regulatory and protocol compliance. Responsibilities include verifying clinical data accuracy, managing investigational products, and maintaining the Investigator Site File.

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CRA II - Italia home based

Syneos Health · Full Time · 11 days ago

Syneos Health

🌎 Italy ⭐ 2-5 yrs exp 💼 Others

The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires managing site-level activities, verifying clinical data integrity, and maintaining the Investigator Site File.

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Clinical Trial Manager ll, Home based Hungary

Syneos Health · Full Time · 11 days ago

Syneos Health

🌎 Hungary ⭐ 5-10 yrs exp 💼 Healthcare

Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing clinical project teams, tracking study progress against milestones, and ensuring regulatory compliance and data integrity.

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Clinical Trial Manager II, Home based Poland

Syneos Health · Full Time · 11 days ago

Syneos Health

🌎 Poland ⭐ 5-10 yrs exp 💼 Healthcare

Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing project milestones, budgets, and ensuring protocol and GCP compliance while leading clinical team members.

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Clinical Trial Manager ll, Home based Bulgaria

Syneos Health · Full Time · 11 days ago

Syneos Health

🌎 Bulgaria ⭐ 5-10 yrs exp 💼 Healthcare

Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing clinical teams, tracking project milestones, and ensuring protocol and regulatory compliance to maintain data integrity and patient safety.

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Clinical Trial Manager ll, Home based Serbia

Syneos Health · Full Time · 11 days ago

Syneos Health

🌎 Serbia ⭐ 5-10 yrs exp 💼 Healthcare

Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves tracking study progress against milestones, managing resource allocation for CRAs, and ensuring regulatory compliance and data integrity.

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Clinical Site Contracts Specialist or Lead USA experience Home Based Brazil

Syneos Health · Full Time · 11 days ago

Syneos Health

🌎 Brazil ⭐ 5-10 yrs exp 💼 Healthcare

Manages the negotiation and execution of clinical study agreements (CTAs) and investigator grant budgets on a study level. Coordinates between internal stakeholders and sponsors to ensure contractual templates align with global strategies and regulatory requirements.

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Senior Medical Writer - Early Phase (Single Sponsor Support)

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Support

Leads the creation and accurate completion of medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and clients to ensure scientific clarity and adherence to regulatory standards.

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Senior Medical Writer - Early phase

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Writing

Leads the creation and completion of high-quality medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and clients to ensure scientific accuracy and adherence to regulatory standards.

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Sr. Medical Writer (Publications)

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Canada ⭐ 5-10 yrs exp 💼 Writing

Leads the creation and accurate completion of medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and mentors junior writers to ensure scientific clarity and adherence to regulatory standards.

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Principal Medical Writer - Publications

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 United Kingdom ⭐ 2-5 yrs exp 💼 Writing

Leads the creation and accurate completion of medical writing deliverables, including protocols, clinical study reports, and manuscripts. Coordinates with cross-functional teams and clients to ensure scientific clarity and adherence to regulatory standards.

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Clinical Trial Manager - Full Service

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Healthcare

The role is responsible for overseeing site management, clinical monitoring, and regulatory compliance to ensure patient safety and data integrity. It involves coordinating with functional leaders to meet study milestones and managing the performance of CRAs and Central Monitors.

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Clinical Operations Manager (Data Review) - UK (homebased)

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 United Kingdom ⭐ 5-10 yrs exp 💼 Healthcare

The role is responsible for managing a multifunctional team to ensure quality deliverables and compliance with customer KPIs. It involves providing line management, overseeing professional development, and managing customer escalations.

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Per Diem Research Nurse London UK

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 United Kingdom ⭐ 2-5 yrs exp 💼 Healthcare

The role involves coordinating and completing clinical trial visits both on and off-site while ensuring strict adherence to trial protocols and SOPs. Responsibilities include administering medication, processing samples, and accurately reporting adverse events to the project management team.

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Independent Contractor Research Nurse - ULM Germany

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Healthcare

The role involves coordinating and completing clinical trial visits both on-site and off-site while ensuring strict adherence to protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events to the project management team.

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Local Contract Research Nurse (Per Diem) - Turin, Italy

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Italy ⭐ 2-5 yrs exp 💼 Healthcare

Coordinate care and facilitate communication between patients and healthcare providers for clinical research studies. Monitor patient progress and collect accurate data while ensuring compliance with regulatory standards and study protocols.

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Senior Principal Statistical Programmer (SAS Viya, R, Python - Europe Only)

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 United Kingdom ⭐ 10+ yrs exp 💼 Software Development

Lead the migration to SAS Viya and provide high-level technical expertise in statistical programming to generate summary tables, listings, and datasets. Mentor team members and ensure all deliverables comply with industry standards and regulatory requirements.

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CTM II

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Germany ⭐ 5-10 yrs exp 💼 Others

Responsible for overseeing site management, clinical monitoring, and data integrity to ensure patient safety and regulatory compliance. This includes managing CRAs, developing clinical monitoring plans, and collaborating with functional leaders to meet study milestones.

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CRA I/II - Beijing

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

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SMA in RWLP- Guangzhou, China, home-based

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

The role involves collaborating with a Clinical Solutions team to shape drug development solutions that meet customer needs. The employee will work within a fully-integrated life sciences services organization to accelerate patient progress.

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Sr. Medical Writer (Regulatory)

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Canada, United Kingdom, United States 💵 $80600 - $175K per year ⭐ 5-10 yrs exp 💼 Legal

Leads the creation and accurate completion of regulatory medical writing deliverables, including protocols, clinical study reports, and NDA submissions. Coordinates with cross-functional teams and clients to ensure documents meet regulatory standards and are delivered on time and budget.

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Senior Medical Editor (Publications)

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Norway 💵 $62000 - $175K per year ⭐ 5-10 yrs exp 💼 Writing

The role involves copyediting and quality reviewing complex medical writing deliverables to ensure accuracy and adherence to AMA and regulatory standards. Additionally, the Senior Medical Editor serves as a project lead, mentoring staff and managing timelines and budgets for assigned projects.

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Sr CTM - Home Based in SPAIN. FSP. Oncology experience is required..

Syneos Health · Full Time · 13 days ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Others

Responsible for site management oversight, clinical monitoring, and ensuring protocol and GCP compliance with a focus on patient safety and data integrity. The role involves managing clinical project teams, mitigating risks, and collaborating with functional leaders to meet study milestones.

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CRA II - Sponsor Dedicated - Oncology / Neurology (Home-Based: Savannah, GA / Augusta, GA / Charleston, SC)

Syneos Health · Full Time · 13 days ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

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CRA II - Sponsor Dedicated - Oncology / Neurology (Home-Based - Boston, MA)

Syneos Health · Full Time · 13 days ago

Syneos Health

🌎 United States ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

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Sr Medical Scientist - Min 3 years of previous experience in development of protocol design - English Advanced - 100% Remote

Syneos Health · Full Time · 14 days ago

Syneos Health

🌎 Argentina, Chile, Mexico, Peru ⭐ 2-5 yrs exp 💼 Design

Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Act as the primary interface between internal teams, customers, and vendors to ensure project milestones and data integrity are met.

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Sr Medical Scientist - Min 3 years of previous experience in development of protocol design - English Advanced - Brasil, 100% Remote

Syneos Health · Full Time · 14 days ago

Syneos Health

🌎 Brazil ⭐ 2-5 yrs exp 💼 Design

Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Act as the primary interface between internal teams, customers, and vendors to ensure data integrity and subject safety.

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Principal Statistical Programmer, SDTM and ADaM. Sponsor Dedicated

Syneos Health · Full Time · 14 days ago

Syneos Health

🌎 United Kingdom ⭐ 10+ yrs exp 💼 Software Development

Lead the development of custom programming code to generate summary tables, listings, and datasets according to statistical analysis plans. Act as a technical subject matter expert for CDISC standards and oversee the programming activities of other personnel to ensure regulatory compliance.

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Principal Statistical Programmer (SDTM)

Syneos Health · Full Time · 14 days ago

Syneos Health

🌎 India ⭐ 10+ yrs exp 💼 Software Development

The role involves developing custom SAS code to generate summary tables, listings, and datasets according to statistical analysis plans. As a lead programmer, the candidate will direct programming activities, ensure quality standards, and mentor junior personnel.

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Sr Clin Ops Specialist in Site Payments - Sponsor dedicated - Home Based in France

Syneos Health · Full Time · 15 days ago

Syneos Health

🌎 France ⭐ 2-5 yrs exp 💼 Others

The role involves creating and updating payment trackers, processing invoices in GMS, and managing patient reimbursement costs. Additionally, the specialist is responsible for mentoring junior payment Clinical Trial Assistants.

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Site Contracts Specialist - Sponsor dedicated - Home Based France

Syneos Health · Full Time · 15 days ago

Syneos Health

🌎 France ⭐ 5-10 yrs exp 💼 Others

Administers contract management processes for clinical trials, including negotiating budgets and preparing site-specific contracts. Collaborates with legal, finance, and clinical operations to ensure timely execution and archival of agreements.

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Sr Clin Ops Specialist in Site Payments FSP, based in France

Syneos Health · Full Time · 15 days ago

Syneos Health

🌎 France ⭐ 5-10 yrs exp 💼 Others

The role involves creating and updating payment trackers and processing invoices and payments within the GMS system. Additionally, the specialist manages patient reimbursement costs and provides mentoring to junior payment CTAs.

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CRA - Sponsor dedicated - Based in Paris Area

Syneos Health · Full Time · 15 days ago

Syneos Health

🌎 France ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

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Principal Clinical Trial Regulatory Affairs - +4 years of experience in regulatory submissions in US/CAN

Syneos Health · Full Time · 16 days ago

Syneos Health

🌎 Argentina ⭐ 5-10 yrs exp 💼 Legal

Acts as a Regulatory Subject Matter Expert to lead clinical trial regulatory activities and manage the site activation pathway. Responsibilities include overseeing regulatory submissions, managing staff, and maintaining strategic client relationships to ensure project deliverables are met.

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Senior Project Specialist (Clinical Trial Assistant) – Bilingual English/French Preferred (Sponsor Dedicated/Remote -Canada)

Syneos Health · Full Time · 18 days ago

Syneos Health

🌎 Canada ⭐ 2-5 yrs exp 💼 Product

The role focuses on managing Trial Master Files (TMF) within Veeva Vault and coordinating clinical study documentation to ensure inspection readiness. It also involves tracking study milestones, supporting site activation, and providing operational project administration for global clinical trials.

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Director, Epidemiology RWE (Immunology or Oncology)

Syneos Health · Full Time · 18 days ago

Syneos Health

🌎 Netherlands ⭐ 5-10 yrs exp 💼 Others

Lead the design and execution of epidemiological and data science projects to generate Real World Evidence for Oncology or Immunology. Develop study protocols, analysis plans, and regulatory documents while managing the identification of fit-for-purpose data sources.

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SSU Regulatory Coordinator

Syneos Health · Full Time · 18 days ago

Syneos Health

🌎 United States 💵 $35600 - $60400 per year ⭐ 0-2 yrs exp 💼 Legal

Support site start-up activities by managing regulatory documentation, clinical trial agreements, and contract logistics. Coordinate the execution of CDAs and NoTs while maintaining internal project trackers and ensuring compliance with SOPs.

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Sr Director, Epidemiology RWE, Sponsor-dedicated - Poland, UK, Romania, Bulgaria, Spain

Syneos Health · Full Time · 18 days ago

Syneos Health

🌎 Bulgaria, Oman, Poland, Romania, Spain, United Kingdom ⭐ 10+ yrs exp 💼 Others

Provides scientific oversight and expertise for Real World Evidence projects, including the development of protocols and study reports. Collaborates with management to win global business opportunities and maintains relationships with sponsors and clinical investigators.

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Senior Site Activation Specialist - Sponsor dedicated - Based in Belgium

Syneos Health · Full Time · 18 days ago

Syneos Health

🌎 Belgium ⭐ 5-10 yrs exp 💼 Others

The role involves managing site activation processes within a sponsor-dedicated environment to accelerate drug development. The specialist will collaborate with cross-functional teams to ensure efficient trial site setup and progress.

agile organization compliance

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CRAI/CRAII

Syneos Health · Full Time · 18 days ago

Syneos Health

🌎 Czech Republic ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and maintain essential trial documentation.

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CTM I - Shanghai

Syneos Health · Full Time · 18 days ago

Syneos Health

🌎 China ⭐ 0-2 yrs exp 💼 Others

The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires managing site-level activities, verifying clinical data accuracy, and maintaining the Investigator Site File.

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Senior Site Contract Specialist (Sponsor-Dedicated/ Remote- Canada)

Syneos Health · Full Time · 18 days ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Legal

Develop, negotiate, and execute Clinical Trial Agreements and budgets while managing financial aspects throughout the study lifecycle. Act as a key liaison between Clinical Operations, Finance, Legal, and investigative sites to ensure successful trial execution.

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Clinical Research Associate - Sponsor Dedicated - Bilingual

Syneos Health · Full Time · 19 days ago

Syneos Health

🌎 Canada ⭐ 5-10 yrs exp 💼 Healthcare

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File and Trial Master File.

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CRA II

Syneos Health · Full Time · 19 days ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory requirements. Develop monitoring tools and collaborate with cross-functional teams to support clinical trial operations.

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Clinical Trial Manager with focus on Project Management - Sponsor dedicated - Brazil Home Based

Syneos Health · Full Time · 20 days ago

Syneos Health

🌎 Brazil ⭐ 2-5 yrs exp 💼 Product

The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires managing site-level activities, budgets, and timelines while acting as a primary liaison with project site personnel.

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Clinical Trial Manager II. Barcelona or Madrid. FSP

Syneos Health · Full Time · 20 days ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Healthcare

Responsible for site management oversight, clinical monitoring, and ensuring patient safety and data integrity across clinical trials. The role involves managing CRAs, overseeing study deliverables, and collaborating with functional leaders to meet study milestones.

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CRA - Future roles (Portugal)

Syneos Health · Full Time · 20 days ago

Syneos Health

🌎 Portugal ⭐ 2-5 yrs exp 💼 Others

The CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

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Principal Medical Writer

Syneos Health · Full Time · 20 days ago

Syneos Health

🌎 Serbia ⭐ 10+ yrs exp 💼 Writing

Leads the creation and completion of complex medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and clients to ensure scientific accuracy and adherence to regulatory standards.

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Principal Medical Writer

Syneos Health · Full Time · 20 days ago

Syneos Health

🌎 Serbia ⭐ 10+ yrs exp 💼 Writing

Leads the creation and completion of complex medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Manages document strategies and coordinates activities across departments while mentoring junior medical writers.

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Sr Director/Director, Strategy & Planning - Real World Late Phase/Real World Evidence

Syneos Health · Full Time · 21 days ago

Syneos Health

🌎 Colombia ⭐ 10+ yrs exp 💼 Others

Lead pre-award strategy and commercial leadership for Real World Late Phase (RWLP) accounts, including RFP strategy and budget structures. Serve as the strategic account leader post-award to maintain portfolio performance and sustain senior-level sponsor relationships.

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Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Syneos Health · Full Time · 21 days ago

Syneos Health

🌎 Canada ⭐ 5-10 yrs exp 💼 Legal

The role involves executing global regulatory CMC strategies and preparing documentation for small molecule products. It also provides regulatory guidance to cross-functional teams to ensure compliance with global requirements.

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Clinical Trial Manager with at least 5 years of experience in clinical research and experience as a CTM working with US - Mexico Home Based

Syneos Health · Full Time · 21 days ago

Syneos Health

🌎 Mexico ⭐ 5-10 yrs exp 💼 Healthcare

The role involves managing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires overseeing data integrity, investigational product reconciliation, and maintaining the Trial Master File.

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Associate Dir, Proposals/RFIs

Syneos Health · Full Time · 22 days ago

Syneos Health

🌎 France 💵 $97300 - $170K per year ⭐ 10+ yrs exp 💼 Others

Lead content governance by establishing editorial standards and managing the enterprise content library for proposals and RFIs. Collaborate with cross-functional teams to develop reusable content and optimize content management platforms using AI tools.

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Sr Medical Director - Immunology/Rheumatology

Syneos Health · Full Time · 22 days ago

Syneos Health

🌎 Spain 💵 $146K - $332K per year ⭐ 10+ yrs exp 💼 Healthcare

Provides medical oversight and monitoring for clinical studies in immunology and rheumatology, including protocol design and drug safety input. Leads medical responses for proposals and mentors staff on therapeutic research principles.

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Proposal Writer

Syneos Health · Full Time · 22 days ago

Syneos Health

🌎 Spain 💵 $56400 - $139K per year ⭐ 0-2 yrs exp 💼 Writing

Leads the development of strategic proposal documents and narratives to win new business awards. Collaborates with internal stakeholders to create customized, high-quality solutions that highlight company differentiation and innovation.

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TMF Specialist (Safety processing) - Min 2 years of previous exp in in central file management - Argentina, 100% home-based

Syneos Health · Full Time · 22 days ago

Syneos Health

🌎 Argentina, Mexico ⭐ 2-5 yrs exp 💼 Others

The role focuses exclusively on processing and reviewing safety documents within the Trial Master File (TMF) system. Responsibilities include ensuring document completeness, indexing accuracy, and collaborating with study owners to resolve discrepancies.

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Regulatory Device CMC Manager

Syneos Health · Full Time · 22 days ago

Syneos Health

🌎 Argentina, Canada, Colombia, Mexico, Serbia ⭐ 5-10 yrs exp 💼 Legal

The Regulatory Device CMC Manager supports strategies for marketed and development products by preparing and submitting regulatory CMC documentation for combination devices. The role provides guidance to cross-functional teams to ensure global regulatory requirements are integrated into development and commercial programs.

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Principal Biostatistician/ Sr Biostatistician (R/Rshiny - EMEA BASED)

Syneos Health · Full Time · 22 days ago

Syneos Health

🌎 Belgium, Greece, Hungary, Ireland, United Kingdom ⭐ 2-5 yrs exp 💼 Healthcare

The role involves serving as a statistical resource to mentor biostatisticians and oversee the preparation of Statistical Analysis Plans and clinical study reports. Additionally, the position focuses on maintaining R-based computing environments and developing Rshiny applications for data visualization.

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Lead CRA (Sponsor dedicated) Belgium

Syneos Health · Full Time · 22 days ago

Syneos Health

🌎 Belgium ⭐ 5-10 yrs exp 💼 Others

Lead and oversee clinical trial site management and monitoring activities for oncology studies to ensure regulatory compliance and data integrity. Responsibilities include conducting oversight visits, mentoring CRAs, and managing relationships with investigators and research networks.

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CRA II or Sr CRA (FSP only BA or FSO any city) - Argentina, home-based - Hiring bonus for new joiners!

Syneos Health · Full Time · 22 days ago

Syneos Health

🌎 Argentina ⭐ 2-5 yrs exp 💼 Recruitment

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and maintain the Investigator Site File and Trial Master File.

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Lead CRA - Sponsor dedicated - Fluent in German and English - Based in Belgium

Syneos Health · Full Time · 22 days ago

Syneos Health

🌎 Belgium ⭐ 5-10 yrs exp 💼 Others

Lead the oversight of clinical trial sites and CRAs, ensuring quality monitoring and compliance across oncology programs. Manage site relationships, conduct oversight visits, and drive continuous improvement of monitoring processes and SOPs.

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Dir, Compensation Infrastructure & Analytics

Syneos Health · Full Time · 25 days ago

Syneos Health

🌎 Serbia ⭐ 10+ yrs exp 💼 Software Development

Oversees global salary structures, market pricing strategies, and job architecture to ensure competitiveness and consistency. Leads pay equity analyses and regulatory compliance while delivering sophisticated compensation analytics for executive leadership.

APPLY

Senior Site Contracts Lead

Syneos Health · Full Time · 25 days ago

Syneos Health

🌎 Serbia ⭐ 5-10 yrs exp 💼 Others

Oversees the negotiation and execution of Clinical Study Agreements (CTAs) and investigator grant budgets on a global scale. Acts as a subject matter expert to resolve contracting issues and aligns CTA strategies with overall study start-up plans.

APPLY

PCS Project Manager

Syneos Health · Full Time · a month ago

Syneos Health

🌎 United States ⭐ 5-10 yrs exp 💼 Product

The PCS Project Manager will lead clinical solutions and partner with innovators across the drug development and commercialization continuum. They are responsible for shaping solutions that meet customer needs and accelerating the delivery of therapies to patients.

APPLY

Permanent Part Time Research Nurse with Data Entry Experience in Oncology - Malaga (Spain)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Data Entry

The role involves coordinating and completing subject trial visits both on- and off-site while ensuring accurate data collection and medication administration. The nurse is responsible for maintaining trial documentation, reporting adverse events, and assisting with patient recruitment in oncology studies.

APPLY

Permanent Part Time Research Nurse with Data Entry experience in Oncology - Madrid (Spain)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Data Entry

The role involves coordinating clinical trial visits and administering trial medications while ensuring accurate data collection in Case Report Forms. The nurse will also manage sample dispatch and report adverse events in compliance with SOPs and GCP guidelines.

APPLY

Independent Contractor Research Nurse - Munich Germany

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Healthcare

The role involves coordinating and completing subject trial visits both on- and off-site while ensuring adherence to trial protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events to the site team.

APPLY

Sr.Stat programmer clin pharm

Syneos Health · Full Time · a month ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Software Development

Develop custom programming code using SAS to generate summary tables, listings, and datasets according to statistical analysis plans. Act as the lead statistical programmer by directing personnel, reviewing project documentation, and ensuring quality standards are met.

APPLY

Independent Contractor Research Nurse - Munich, Germany

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Healthcare

The role involves coordinating and completing subject trial visits both on and off-site while ensuring adherence to trial protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events.

APPLY

Regulatory Senior Consultant

Syneos Health · Full Time · a month ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Legal

The role involves partnering with innovators across the drug development and commercialization continuum to navigate regulatory complexities. The consultant will collaborate with specialized teams to deliver unique insights and accelerate the delivery of therapies to patients.

APPLY

CRA II - Sponsor-dedicated (Poland)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Poland ⭐ 2-5 yrs exp 💼 Others

The CRA II is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File and Trial Master File.

APPLY

Principal Biostatistician Medical Affairs ( UK, Ireland, Poland, Greece, Hungary, Romania, Ukraine, South Africa, Belgium, Netherlands)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Belgium, France, Hungary, Ireland, United Kingdom ⭐ 10+ yrs exp 💼 Healthcare

Provide statistical support to the Medical Affairs group focusing on exploratory analysis, observational studies, and real-world evidence. Manage the statistical lifecycle of projects from protocol development to the final clinical study report.

APPLY

CRA II Germany - eastern Germany (Leipzig, Halle, Berlin)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and maintain the Investigator Site File.

APPLY

Site Contracts Specialist with experience in Clinical Trials, Home-Based Mexico, Brazil and Argentina

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Brazil, Mexico ⭐ 5-10 yrs exp 💼 Healthcare

Administers contract management processes for clinical trials, including negotiating budgets and preparing agreements for investigators and vendors. Coordinates with legal and finance departments to ensure the execution and archival of Clinical Trial Agreements (CTAs).

APPLY

Clinical Trial Manager II (Sponsor dedicated) - Experience in project management and previous experience as CRA - Chile Home Based

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Chile ⭐ 5-10 yrs exp 💼 Product

Oversee site management, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Coordinate with functional leaders to meet study milestones and manage the clinical project team's contractual obligations.

APPLY

Safety & PV Specialist I - Mexico Remote

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Mexico ⭐ 0-2 yrs exp 💼 Others

The specialist is responsible for processing Individual Case Safety Reports (ICSRs), including data entry, coding, and narrative summaries in safety databases. They also ensure regulatory compliance through literature screening, xEVMPD validation, and maintaining the Trial Master File.

APPLY

Clinical Trial Manager with focus on project management - Sponsor dedicated - Argentina Home Based

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Argentina ⭐ 5-10 yrs exp 💼 Product

Responsible for overseeing site management, clinical monitoring, and data integrity to ensure patient safety and regulatory compliance. The role involves managing clinical project teams, mitigating risks, and collaborating with functional leaders to meet study milestones.

APPLY

CRA II - Chengdu

Syneos Health · Full Time · a month ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory requirements. Develop quality monitoring tools and collaborate with cross-functional teams to support clinical trial operations.

APPLY

Clinical Operations Specialist (Sponsor Dedicated) – Remote, Canada (Bilingual English/French)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Canada ⭐ 2-5 yrs exp 💼 Healthcare

The role involves coordinating regulatory submissions to Health Canada, REBs, and IRBs while managing documentation for multiple active clinical protocols. It also includes processing clinical trial invoices and supporting study start-up and closeout activities to ensure compliance.

APPLY

Site Contracts Specialist (Polish Required)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Serbia ⭐ 5-10 yrs exp 💼 Others

Administers all contract management processes for clinical trials, including negotiating budgets and preparing agreements for investigators and vendors. Collaborates with legal and finance departments to ensure compliance with timelines and quality standards.

APPLY

Regulatory Consultant

Syneos Health · Full Time · a month ago

Syneos Health

🌎 India ⭐ 2-5 yrs exp 💼 Legal

The role involves preparing and managing regulatory submissions, including CMC sections and post-approval variations for EU and GCC markets. The consultant will act as a subject matter expert, conducting gap analyses and supporting multidisciplinary project teams throughout the product life cycle.

APPLY

CRA II/ SCRA I

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Australia ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain essential study documentation.

APPLY

CRA II/ SCRA

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Australia ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain essential trial documentation.

APPLY

CRA II/Snr CRA

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Australia ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

APPLY

CRA II- SCRA I

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Australia ⭐ 2-5 yrs exp 💼 Others

The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires managing site-level activities, verifying clinical data integrity, and maintaining the Investigator Site File.

APPLY

Central Report Reviewer

Syneos Health · Full Time · a month ago

Syneos Health

🌎 India ⭐ 2-5 yrs exp 💼 Others

Responsible for executing central report review activities to ensure patient safety, data integrity, and regulatory compliance. This includes reviewing site monitoring documentation and escalating serious issues to project management.

APPLY

Clinical Sr Project Manager / Assoc Director (Global role, Multisponsor) ** Remote US & Canada **

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Spain ⭐ 10+ yrs exp 💼 Product

Lead the operational and financial delivery of global clinical projects from proposal to final deliverables. Act as the primary liaison between the company and customers while managing interdisciplinary teams and ensuring regulatory compliance.

APPLY

Sr.CRA II - Warsaw

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Poland ⭐ 5-10 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, data integrity, and investigator relationships while providing mentorship to junior CRAs.

APPLY

Mgr, QA & Reg Compliance - Shanghai/Beijing

Syneos Health · Full Time · a month ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Legal

Manage quality assurance and regulatory compliance within the clinical solutions team to accelerate drug development. Collaborate with cross-functional teams to ensure customer success and adherence to healthcare regulations.

APPLY

Site Contracts Specialist II/Sr - China

Syneos Health · Full Time · a month ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Others

Administers contract management processes for clinical trials, including negotiating budgets and preparing agreements for investigators and vendors. Collaborates with legal and finance departments to ensure compliance and timely execution of site-specific contracts.

APPLY

Sr CRA I / II (preferred base Cape Town) Sponsor dedicated

Syneos Health · Full Time · a month ago

Syneos Health

🌎 South Africa ⭐ 5-10 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, data integrity, and investigator relationships while providing mentorship to junior CRAs.

APPLY

Medical Writing + Research Manager, RWE (Epidemiology) - (study protocols, SAPlans, study reports, abstracts)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Bulgaria, Colombia, Hungary, Mexico, Oman, Romania ⭐ 5-10 yrs exp 💼 Healthcare

The role focuses on medical writing and supporting the design and execution of Real World Evidence studies, including protocols and reports. It involves collaborating with cross-functional teams to ensure scientific rigor and managing project outputs within budget and timelines.

APPLY

Senior Site Contracts Manager (Sponsor Dedicated /Remote – US Based)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Spain 💵 $79800 - $139K per year ⭐ 5-10 yrs exp 💼 Others

The role involves developing, negotiating, and managing US site budgets and clinical trial agreements for Pharma and Vaccine studies. The manager will lead negotiations with academic institutions and ensure contracts balance business objectives with legal protections.

APPLY

Senior/ Principal Statistical Programmer (R/RShiny)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Armenia, Greece, Hungary, Oman, Romania, Serbia ⭐ 5-10 yrs exp 💼 Software Development

Develop custom programming code using R/RShiny to generate summary tables, listings, and graphs according to statistical analysis plans. Act as a lead programmer by directing activities, reviewing project documentation, and mentoring junior personnel.

APPLY

Medical Scientist

Syneos Health · Full Time · a month ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Healthcare

The Medical Scientist will collaborate with clinical solutions teams to accelerate drug development and commercialization for customers. They will apply deep therapeutic expertise to shape solutions that improve patient progress and healthcare outcomes.

APPLY

Per Diem - Freelance Research Nurse - Lille (France)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 France ⭐ 2-5 yrs exp 💼 Healthcare

The role involves coordinating and completing clinical trial visits both on-site and off-site while ensuring strict adherence to protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events.

APPLY

Local Contractor - Research Nurse (per diem) - Lavaveix-Les-Mines area (France)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 France ⭐ 2-5 yrs exp 💼 Healthcare

The Research Nurse is responsible for coordinating and completing subject trial visits both on and off-site while ensuring adherence to trial protocols and SOPs. Key duties include administering trial medication, processing samples, and accurately reporting adverse events to the site team.

APPLY

eCOA Project Manager with at least 2 years of experience in Clinical Trials & eCOA technologies - Argentina Home Based

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Argentina ⭐ 2-5 yrs exp 💼 Product

The eCOA Manager is responsible for the end-to-end planning, implementation, and oversight of electronic Clinical Outcome Assessment solutions across clinical trials. This includes leading delivery activities from startup to close-out and serving as the primary liaison with eCOA vendors.

APPLY

CRA Real World Late Phase - Germany

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, data integrity, and subject safety for Real World Late Phase studies.

APPLY

Clinical Research Associate (CRA) Germany

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Healthcare

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

APPLY

Medical Director- Psychiatry (US Based Only - Board-certified in Psychiatry is required)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Spain 💵 $146K - $332K per year ⭐ 10+ yrs exp 💼 Healthcare

Provides medical oversight and monitoring for assigned clinical studies, serving as the primary medical contact for customers. Responsible for protocol design, drug safety oversight, and delivering therapeutic training to project teams.

APPLY

Real World Biostatistician - RWE CMH experience

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Spain, United States ⭐ 5-10 yrs exp 💼 Healthcare

Design and execute real-world evidence studies using EMR and claims data to inform clinical development and regulatory strategy. Develop robust statistical methodologies and translate complex analytical results into actionable insights for cross-functional stakeholders.

APPLY

CRA II/Sr CRA based in Berlin or Hamburg

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

APPLY

Pr Statistical Programmer(ADAM, TLF, SDTM)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 India ⭐ 10+ yrs exp 💼 Software Development

Develop custom SAS programming code to generate summary tables, listings, and datasets according to statistical analysis plans. Act as a lead statistical programmer by directing activities, reviewing project documentation, and ensuring CDISC compliance.

APPLY

Medical Writer- Future Roles (India)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 India ⭐ 2-5 yrs exp 💼 Writing

Lead the creation and accurate completion of medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinate with cross-functional teams and clients to ensure scientific clarity and adherence to regulatory standards.

APPLY

Regulatory Consultant - CMC (CMC with small molecule products)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Portugal, Serbia, Spain, United Kingdom ⭐ 5-10 yrs exp 💼 Legal

The consultant will support global regulatory CMC for marketed small molecule products, focusing on lifecycle management and submissions for the Middle East and North Africa. They will review CMC sections of submissions and collaborate with cross-functional teams to develop regulatory strategies.

APPLY

Principal Statistical Programmer (US, CAD, UK only)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Canada ⭐ 10+ yrs exp 💼 Software Development

The role involves developing custom SAS code to generate summary tables, listings, and graphs while ensuring compliance with statistical analysis plans and regulatory guidelines. The Principal Statistical Programmer also acts as a lead, directing programming activities and mentoring junior personnel.

APPLY

Mgr, Accounting

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Finance

The role is responsible for preparing SR&ED tax incentive claims and leading income and indirect tax audits. It also involves managing monthly, quarterly, and year-end closes while ensuring compliance with US and Canadian GAAP and Sarbanes-Oxley controls.

APPLY

Feasibility Strategy Analytics Lead (Sponsor dedicated) - Argentina, Brazil and Mexico Home Based

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Argentina, Brazil, Mexico ⭐ 5-10 yrs exp 💼 Software Development

Lead global feasibility business deliverables by analyzing data to develop country and site strategies for clinical trial proposals. Collaborate with internal stakeholders to review sponsor requirements and provide intelligence on patient access and enrollment modelling.

APPLY

Regulatory CMC Manager Cell and Gene Therapy

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Argentina, Brazil, Colombia, Mexico, Serbia ⭐ 5-10 yrs exp 💼 Legal

The Regulatory CMC Manager supports global regulatory CMC strategies for cell and gene therapy products during development and commercialization. This includes preparing regulatory documentation and providing guidance to cross-functional teams on compliance and GMP investigations.

APPLY

Clinical Research Associate - Canada

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Healthcare

The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires managing site-level activities, verifying clinical data integrity, and overseeing investigational product inventory.

APPLY

Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Denmark, France, Greece, Hungary, United Kingdom ⭐ 5-10 yrs exp 💼 Software Development

Provides comprehensive statistical support throughout the project lifecycle, from protocol development to the final clinical study report. Coordinates biostatistics and programming personnel to ensure high-quality deliverables and maintains inspection readiness.

APPLY

CRA II - FSP - Istanbul or Ankara

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Turkey ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain essential trial documentation.

APPLY

Site Activation Manager assigned to Client

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Mexico ⭐ 5-10 yrs exp 💼 Others

Lead and manage Site Start-Up (SSU) deliverables globally or regionally to ensure study sites are activation-ready on time and within budget. Oversee the entire lifecycle from site selection and regulatory submissions to the collection of essential documents.

APPLY

Biostatistician- Future Roles (India)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Healthcare

The role involves providing statistical support throughout the project lifecycle, from protocol development to the creation of Clinical Study Reports. Key duties include preparing Statistical Analysis Plans, coordinating biostatistics personnel, and ensuring the quality of project deliverables.

APPLY

Clinical Research Associate - Full-Service

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Healthcare

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

APPLY

Experienced Clinical Research Associate - Sponsor Dedicated

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Healthcare

The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying clinical data integrity, managing investigational products, and maintaining the Trial Master File.

APPLY

Central Monitor II - Remote Mexico

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Mexico ⭐ 2-5 yrs exp 💼 Others

Perform remote patient data review for Phase I-IV clinical research to ensure protocol compliance and data integrity. Identify safety concerns and protocol deviations while communicating issues to the project team for action.

APPLY

CRA I Germany

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Germany ⭐ 0-2 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File and Trial Master File.

APPLY

CRA Germany - multi-sponsor (north-east Germany)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Others

The CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

APPLY

CRA II Germany - multisponsor

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

APPLY

CRA Austria

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Austria ⭐ 2-5 yrs exp 💼 Others

The CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

APPLY

CRA II - SR CRA Brazil

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Brazil ⭐ 5-10 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and provide guidance to site staff and junior CRAs.

APPLY

Employee Wellness Specialist

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

The Employee Wellness Specialist focuses on enhancing employee well-being within a global life sciences services organization. The role involves collaborating with diverse teams to support a healthy and inclusive corporate culture.

APPLY

CRA II - Shenyang

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory requirements. Develop quality monitoring tools and collaborate with cross-functional teams to support smooth clinical trial operations.

APPLY

Assessment Scientist: Masters in Psychology; Psychometrists

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Serbia ⭐ 2-5 yrs exp 💼 Others

Lead the scientific oversight of eCOA implementation and manage the licensing, translation, and integrity of clinical outcome assessment scales. Design and deliver rater training programs to ensure standardized endpoint data collection across clinical sites.

APPLY

Sr CRA – Minimum 4 Years of CRA Experience is a Must - Riyadh

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Saudi Arabia ⭐ 2-5 yrs exp 💼 Others

The Senior CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They must manage site performance, verify clinical data integrity, and oversee the handling of investigational products.

APPLY

Sr Statistical Programmer (NA Only)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Spain 💵 $80600 - $145K per year ⭐ 5-10 yrs exp 💼 Software Development

Develop custom SAS code to generate summary tables, listings, and graphs according to statistical analysis plans. Act as a lead programmer by directing activities, reviewing project documentation, and mentoring junior personnel.

APPLY

Internal Account Director - Recruitment & Retention Strategy

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Bulgaria, El Salvador, Serbia, Slovakia, Spain ⭐ 5-10 yrs exp 💼 Sales

The role involves managing recruitment and retention strategies from planning to close-out, including the creation of Patient Recruitment Plans. The Director will represent R&R services at bid defense meetings and collaborate with internal teams to ensure timely enrollment and risk mitigation.

APPLY

Manager, Biostatistics

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 United Kingdom ⭐ 5-10 yrs exp 💼 Others

Responsible for hiring, managing, and developing biostatisticians while ensuring projects meet timelines, budgets, and quality standards. The role involves overseeing staff performance, mentoring associates, and managing client relationships to ensure successful project execution.

APPLY

Site Contracts Specialist II/Sr - Sponsor dedicated

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Malaysia, Taiwan ⭐ 5-10 yrs exp 💼 Others

Administers contract management processes and negotiates budgets and contracts for industry-sponsored clinical trials. Collaborates with legal, finance, and clinical operations to ensure timely execution and archival of Clinical Trial Agreements.

APPLY

Principal Statistician Oncology with Submission Experience

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Denmark, France, Greece, Hungary, United Kingdom ⭐ 10+ yrs exp 💼 Software Development

The role involves leading statistical activities across the clinical trial lifecycle, from protocol development to the final clinical study report. Responsibilities include mentoring biostatisticians, overseeing SAP preparation, and managing regulatory submission requirements.

APPLY

R Statistical Programmer - Submission Experience Required (hiring in Armenia, UK, India, SA)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Armenia, India, South Africa, United Kingdom ⭐ 5-10 yrs exp 💼 Software Development

Develop custom programming code using R or SAS to generate summary tables, listings, and datasets for clinical trials. Act as a lead statistical programmer, overseeing deliverables, ensuring CDISC compliance, and mentoring junior staff.

APPLY

Local Contractor Research Nurse (Per Diem)- Paris (France)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 France ⭐ 2-5 yrs exp 💼 Healthcare

The role involves coordinating and completing subject trial visits both on- and off-site while ensuring adherence to trial protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events.

APPLY

Principal Biostatistician - Biomarker (EMEA Remote)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Germany, Hungary, Ireland, Spain ⭐ 10+ yrs exp 💼 Healthcare

Collaborate with cross-functional teams to plan, execute, and analyze biomarker and genomics aspects of clinical studies. Develop Biomarker Evaluation Plans and reports while implementing standard processes for routine biomarker assessments.

APPLY

Site Contracts Lead - Shanghai

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Others

Lead site contracts within the clinical solutions team to accelerate drug development and commercialization. Collaborate with cross-functional teams to shape solutions that meet customer needs and improve patient progress.

APPLY

Project Manager II - Shanghai or Beijing

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Product

Lead interdisciplinary clinical research studies ensuring compliance with GCP, SOPs, and regulatory requirements while managing timelines and budgets. Act as the primary liaison between the company and customers to ensure successful study launch, conduct, and closeout.

APPLY

Medical Writer II (MLR Reviewer +Veeva)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 India ⭐ 2-5 yrs exp 💼 Writing

Lead and manage medical writing activities for clinical studies, including the development of manuscripts, abstracts, and posters. Coordinate with cross-functional teams to ensure scientific accuracy and adherence to regulatory standards and branding.

APPLY

Project Manager II

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Product

Manage interdisciplinary clinical research studies ensuring compliance with GCP and regulatory requirements while acting as the primary liaison for customers. Lead project teams to oversee quality, timelines, and financial performance of assigned projects.

APPLY

Clinical Scientist - Respiratory

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Healthcare

Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and deliverables while interfacing between internal teams, customers, and vendors to ensure data integrity and subject safety.

APPLY

Clinical Scientist - Vaccine

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Healthcare

Collaborates with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manages project scope and serves as the primary interface between internal teams, customers, and vendors regarding eligibility and data review.

APPLY

Clinical Scientist - Cardiovascular

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Healthcare

Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and deliverables while interfacing between internal teams, customers, and vendors to ensure data integrity and subject safety.

APPLY

Clinical Scientist - Ophthalmology

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Healthcare

Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and serve as the primary interface between internal teams, customers, and vendors regarding eligibility and data review.

APPLY

Clinical Scientist - Immunology (Expertise in Ulcerative Colitis, Crohn’s disease and Rheumatology + Excel)

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Healthcare

Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and deliverables while interfacing between internal teams, customers, and vendors to ensure data integrity and subject safety.

APPLY

Sr RW Programmer/Sr Data Scientist/Analyst - Real World Data(US and UK Only)

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain 💵 $80600 - $145K per year ⭐ 5-10 yrs exp 💼 Software Development

Develop programs and provide statistical support for epidemiologists to source, organize, and interpret complex real-world data sets. Create analysis datasets, tables, and figures while ensuring outputs meet quality standards and protocol requirements.

APPLY

Study Manager - Cardiovascular

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Others

Manage interdisciplinary clinical research studies ensuring compliance with GCP, SOPs, and regulatory requirements. Act as the primary liaison between the company and customers to oversee study launch, conduct, closeout, and financial performance.

APPLY

Study Manager - Immunology

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Others

Manage interdisciplinary clinical research studies ensuring compliance with GCP, SOPs, and regulatory requirements. Act as the primary liaison between the company and customers to oversee study launch, conduct, closeout, and financial performance.

APPLY

Study Manager - Ophthalmology

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Others

The Study Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing timelines and budgets. They act as the primary liaison between the company and the customer to ensure successful study launch, conduct, and closeout.

APPLY

Study Manager - Respiratory

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Others

The Study Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing timelines and budgets. They act as the primary liaison between the company and the customer to ensure successful study launch, conduct, and closeout.

APPLY

Study Manager - Oncology

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Others

Manage interdisciplinary clinical research studies in oncology, ensuring compliance with GCP and regulatory requirements. Act as the primary liaison between the company and customers to oversee study launch, conduct, and financial performance.

APPLY

Study Manager - Vaccine

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Others

Manage interdisciplinary clinical research studies ensuring compliance with GCP and regulatory requirements while acting as the primary liaison for customers. Lead project teams to oversee quality, timelines, budget management, and the completeness of the Trial Master File.

APPLY

Site Activation Specialist I/II - Guangzhou

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Responsible for managing site activation and quality deliverables at the country level, including regulatory submissions and essential document collection. Acts as a subject matter advisor for in-country performance and supports site selection, contract negotiation, and budget management.

APPLY

Sr Clinical Operation Specialist / Lead Clinical Operation Specialist (immediate Joiner)

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Healthcare

Support the setup and maintenance of CTMS and TMF while managing study budgets and external service provider coordination. Perform central monitoring and data oversight to ensure the consistency and correctness of clinical study data.

APPLY

CRA II- SCRA (Melb/ Sydney)

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Australia ⭐ 2-5 yrs exp 💼 Others

Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.

APPLY

Principal Biostatistician(Clinical Pharmacology)

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 India ⭐ 10+ yrs exp 💼 Healthcare

The role involves providing biostatistical expertise within the Clinical Pharmacology domain to accelerate drug development and commercialization. The Principal Biostatistician will collaborate with cross-functional teams to deliver data-driven solutions for healthcare customers.

APPLY

Site Contracts Specialist with CRO/Pharma experience home-based in Serbia

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Serbia ⭐ 2-5 yrs exp 💼 Sales

Lead the negotiation and preparation of contracts and budgets for industry-sponsored clinical trials. Coordinate with legal, finance, and clinical operations to ensure accurate execution and archival of site-specific agreements.

APPLY

SSUS II

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Responsible for quality deliverables and regulatory submissions at the country level to ensure timely site activation. Acts as a subject matter advisor for in-country performance, managing essential document collection and budget negotiations.

APPLY

Director, Business Development

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Switzerland ⭐ 10+ yrs exp 💼 Sales

The Director of Business Development is responsible for driving sales growth in a specific geographic territory through a mix of new client acquisition and existing account expansion. This involves developing tailored engagement plans and collaborating with cross-functional teams to deliver integrated life sciences solutions.

APPLY

Director, Business Development

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Netherlands 💵 $134K - $255K per year ⭐ 10+ yrs exp 💼 Sales

The Director of Business Development will lead initiatives to accelerate customer success in drug development and commercialization. This role involves collaborating with various teams to navigate complexities and drive impactful solutions for healthcare.

APPLY

On-site monitor ** open to diverse EMEA countries **

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Austria, Hungary, Oman, Poland, Romania, Slovakia ⭐ 2-5 yrs exp 💼 Others

Perform site management and monitoring activities in compliance with SOPs, local regulations, and ICH-GCP guidelines. Manage site identification, qualification, start-up, and routine monitoring while ensuring data accuracy and audit readiness.

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West Coast Regional Leader, Business Development

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Netherlands 💵 $193K - $367K per year ⭐ 10+ yrs exp 💼 Sales

Lead business development efforts across the West Coast region to accelerate customer success in the life sciences sector. Partner with innovators to navigate the drug development and commercialization continuum.

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Clinical Assessment Scientist - COA Lead - Sponsor-dedicated (Sweden, Spain, UK, South Africa, Portugal, Denmark)

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Denmark, Portugal, Spain, Sweden ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Assessment Scientist will act as a COA Lead, collaborating with cross-functional teams to deliver clinical solutions for drug development projects. They will apply therapeutic expertise to understand customer needs and drive progress across the drug development continuum.

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Sr.CRA in KSA - Single Sponsor - CKD

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Saudi Arabia ⭐ 5-10 yrs exp 💼 Others

The Senior Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying clinical data accuracy, managing site staff performance, and ensuring the safety and integrity of clinical trial data.

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CRA II

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Australia ⭐ 2-5 yrs exp 💼 Others

The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They also manage site-level activities, verify clinical data accuracy, and provide guidance to site staff to ensure project objectives are met.

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CTM I/II

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Japan ⭐ 5-10 yrs exp 💼 Others

Responsible for site management oversight, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Collaborates with cross-functional teams to manage study milestones, risk mitigation, and clinical trial documentation.

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Dir, Epidemiology Pipeline (TA-Immunology)

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 United States ⭐ 10+ yrs exp 💼 Others

The Director serves as a scientific subject matter expert in immunology, providing oversight for clinical trials and leading the development of global business opportunities. They coordinate with project managers to ensure study quality, manage budgets, and facilitate scientific advisory boards while producing technical reports and manuscripts.

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Dir, Epidemiology Pipeline (TA - Virology)

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 United States ⭐ 10+ yrs exp 💼 Others

The Director serves as a scientific subject matter expert in virology, providing oversight for clinical trials and leading the development of project proposals and bid defenses. They coordinate with project managers to ensure study quality, timelines, and budgets while facilitating scientific advisory boards and authoring industry publications.

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Dir, Epidemiology Pipeline (TA-Oncology)

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 United States ⭐ 10+ yrs exp 💼 Others

The role serves as a scientific subject matter expert in oncology clinical trials, providing oversight for project proposals, study start-up, and ongoing management. It involves collaborating with business development to win global opportunities and leading the development of scientific reports, manuscripts, and study documentation.

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CTM II - Sponsor dedicated - Argentina Home Based

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Argentina ⭐ 5-10 yrs exp 💼 Others

Responsible for site management oversight, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Collaborates with cross-functional teams to manage study milestones, risk mitigation, and clinical trial documentation.

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Principal Site Grant Manager

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Spain 💵 $79800 - $139K per year ⭐ 5-10 yrs exp 💼 Teaching

The Principal Site Grant Manager establishes and maintains investigator budget templates and negotiation strategies while serving as a subject matter expert for global site budgeting issues. They collaborate with internal and external stakeholders to ensure fair market value and operational compliance throughout the clinical trial budget life cycle.

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Clinical Trial Manager

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Trial Manager oversees site management, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. They also manage study risks, coordinate with functional teams, and ensure adherence to contractual obligations and study timelines.

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CRA Switzerland

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Switzerland ⭐ 2-5 yrs exp 💼 Others

The Clinical Research Associate (CRA) is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and ensure the safety and confidentiality of study subjects.

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CRA oncology Germany

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Others

The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site performance, verify clinical data accuracy, and ensure patient safety and data integrity throughout the study.

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Experimented CRA France - single sponsor

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 France ⭐ 2-5 yrs exp 💼 Others

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory guidelines. Collaborate with cross-functional teams and investigators to support clinical trial operations and maintain accurate documentation.

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Site Care Partner I (SrCRA) - FSP, Sponsor Dedicated

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Turkey ⭐ 5-10 yrs exp 💼 Others

The Site Care Partner performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and provide guidance to site staff to ensure project objectives and timelines are met.

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CLINICAL TRIAL MANAGER - FUTURE ROLES

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Brazil ⭐ 2-5 yrs exp 💼 Healthcare

The role involves performing all phases of site monitoring, including qualification, initiation, interim monitoring, and close-out visits, ensuring strict adherence to regulatory guidelines like ICH-GCP and protocol compliance. Key duties include evaluating site performance, managing data integrity through Source Document Review and query resolution, and ensuring proper handling and documentation of the Investigational Product.

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Site Activation - Futures Needs - (Brazil)

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Brazil ⭐ 0-2 yrs exp 💼 Others

The role is responsible for providing quality deliverables at the country level, adhering to project requirements and local rules, while tracking submission/approval timelines and managing basic financial aspects of the project. Specific functions may include Local Submissions Specialist duties, Site ID and Feasibility Support, or Local Investigator Contract and Budget Negotiation.

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CRA - Futures Roles - (BRA)

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Brazil ⭐ 2-5 yrs exp 💼 Others

The role involves performing comprehensive site monitoring activities, including qualification, initiation, monitoring, management, and close-out visits, ensuring strict adherence to regulatory guidelines like ICH-GCP and protocol compliance. Key duties include evaluating site performance, managing data integrity through source document review and query resolution, and ensuring proper handling of investigational products.

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R Statistical Programmer (hiring in Armenia, Hungary, Estonia, CR, Romania, Argentina, Brazil, or Columbia only)

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Armenia, Estonia, Hungary, Oman, Romania ⭐ 5-10 yrs exp 💼 Software Development

The R Statistical Programmer will use R and SAS to develop custom code for generating summary tables, listings, graphs, and derived datasets according to the statistical analysis plan, ensuring outputs meet quality standards. This role involves performing validation programming, resolving discrepancies, managing project timelines, and acting as the lead statistical programmer directing the activities of other personnel.

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Statistical Programmer- Future Roles (India)

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Software Development

The role involves using SAS or other software to develop custom programming code for generating summary tables, data listings, graphs, and derived datasets according to the statistical analysis plan and specifications. Responsibilities also include performing validation programming, ensuring outputs meet quality standards, and managing project timelines while acting as the lead statistical programmer.

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CTM - Future roles (Bulgaria)

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Bulgaria ⭐ 2-5 yrs exp 💼 Others

The role involves performing site qualification, initiation, monitoring, management, and close-out visits while ensuring compliance with regulatory standards like ICH-GCP and protocol requirements. Key duties include evaluating site performance, managing data integrity via Source Document Review and query resolution, and maintaining essential study documentation.

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Sr CRA I - Beijing

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

The role involves performing all stages of site monitoring, including qualification, initiation, interim monitoring, management, and close-out visits, ensuring strict adherence to regulatory guidelines like ICH-GCP and protocol compliance. Key duties include evaluating site performance, verifying data accuracy via Source Document Review, managing query resolution, and ensuring proper handling and documentation of the Investigational Product.

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CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec)

Syneos Health · Full Time · 5 months ago

Syneos Health

🌎 Canada ⭐ 0-2 yrs exp 💼 Others

The role involves performing site qualification, initiation, monitoring, management, and close-out visits, ensuring compliance with regulatory standards like ICH-GCP and protocol requirements. Responsibilities also include evaluating site performance, managing data integrity through source document review and query resolution, and maintaining essential study documentation.

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CRA II (Multi-sponsor) - Ophtalmology experience is required - Brazil Home Based

Syneos Health · Full Time · 5 months ago

Syneos Health

🌎 Brazil ⭐ 2-5 yrs exp 💼 Others

The CRA II performs site qualification, initiation, monitoring, management, and close-out visits ensuring compliance with regulatory standards like ICH-GCP and protocol requirements. Responsibilities also include evaluating site performance, verifying informed consent, assessing patient safety and data integrity, and managing essential study documentation.

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Clinical Trial Manager II

Syneos Health · Full Time · 5 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Trial Manager II is responsible for oversight of site management, clinical monitoring, and central monitoring deliverables, focusing on patient safety, compliance, and data integrity from site activation through closeout. This role involves identifying and mitigating risks to trial deliverables, coordinating with other functional leaders, and ensuring quality control over monitoring documentation and study systems.

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Sr Clinical Trial Manager

Syneos Health · Full Time · 5 months ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Healthcare

This posting is intended for a possible upcoming opportunity, adding interested candidates to a talent pipeline for future consideration as a Sr Clinical Trial Manager. The role involves working alongside industry experts to accelerate the delivery of important therapies to patients.

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IMS Specialist I

Syneos Health · Full Time · 5 months ago

Syneos Health

🌎 Argentina ⭐ 0-2 yrs exp 💼 Others

The job description focuses heavily on the company's mission, culture, and commitment to accelerating therapy delivery rather than listing specific IMS Specialist I tasks. The role is situated within a fully integrated biopharmaceutical solutions organization focused on clinical, medical affairs, and commercial insights.

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Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; US/CAN

Syneos Health · · 5 months ago

Syneos Health

🌎 Canada, Norway, United Kingdom, United States 💵 $80600 - $145K per year ⭐ 5-10 yrs exp 💼 Legal

The role involves leading the clear and accurate completion of medical writing deliverables for studies, managing associated activities, and resolving client comments with minimal supervision. Responsibilities include completing various regulatory documents such as protocols, CSRs, IBs, submissions, and plain language summaries while adhering to regulatory standards and timelines.

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Sr Dir, Business Development

Syneos Health · Full Time · 6 months ago

Syneos Health

🌎 United States 💵 $121K - $306K per year ⭐ 10+ yrs exp 💼 Sales

The Senior Director, Business Development is tasked with driving sales growth within an assigned territory by balancing strategic expansion of existing accounts with the pursuit of new opportunities through tailored engagement plans. Core duties involve developing and executing a comprehensive sales strategy, managing territory performance using data, nurturing key client relationships, and collaborating cross-functionally to co-develop client solutions.

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Head of R&D and Scientific Strategy, Rare Disease

Syneos Health · Full Time · 6 months ago

Syneos Health

🌎 United States ⭐ 10+ yrs exp 💼 Others

The Head of R&D and Scientific Strategy supports or leads matrix teams to drive value by leveraging scientific capabilities, often focusing on cross-functional initiatives and developing innovative solutions for customers under the CSO's guidance. This role involves contributing to scientific communications, engaging with customers, potentially interacting with C-level personnel, and coordinating resources to craft tailored scientific solutions.

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CRA single-sponsor in Germany

Syneos Health · Full Time · 6 months ago

Syneos Health

🌎 Germany ⭐ 2-5 yrs exp 💼 Others

The Clinical Research Associate (CRA) will perform site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulatory and protocol standards. They will assess site performance, manage site-level activities, and support patient recruitment and retention strategies.

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CRA SSU with at least 2 years of regulatory experience - Sponsor dedicated - Argentina Client Based

Syneos Health · Full Time · 6 months ago

Syneos Health

🌎 Argentina ⭐ 2-5 yrs exp 💼 Legal

The CRA SSU is responsible for ensuring quality deliverables at the country level, tracking submission timelines, and monitoring project finances. They also handle local submissions, site activation processes, and act as a liaison between investigational sites and functional leads.

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Principal Biostatistician (Rshiny - EMEA BASED)

Syneos Health · Full Time · 6 months ago

Syneos Health

🌎 Belgium, Greece, Hungary, Ireland, Oman, Poland, Romania, Spain, Ukraine, United Kingdom ⭐ 2-5 yrs exp 💼 Healthcare

The Principal Biostatistician serves as a resource for the statistical department, mentoring biostatisticians and overseeing training plans. They provide support across all statistical tasks during the project lifecycle and ensure high-quality work is completed on time.

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Sr.CRA I or Sr.CRA II- FSP - Romania

Syneos Health · Full Time · 6 months ago

Syneos Health

🌎 Oman, Romania ⭐ 2-5 yrs exp 💼 Others

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with clinical practices and study protocols. Collaborate with cross-functional teams to support clinical trial activities and manage the work of lower-level professionals.

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Senior Site Contracts Lead

Syneos Health · Full Time · 7 months ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Others

The Senior Site Contracts Lead will be responsible for managing site contracts and ensuring compliance with regulatory requirements. This role involves collaborating with various teams to streamline processes and enhance customer success.

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Director, Business Development

Syneos Health · Full Time · 7 months ago

Syneos Health

🌎 Netherlands 💵 $121K - $266K per year ⭐ 5-10 yrs exp 💼 Sales

The Director of Business Development is responsible for driving sales growth across a geographic territory by balancing account farming with new client acquisition. This role involves developing tailored engagement plans and collaborating with cross-functional teams to address client-specific challenges.

salesforce medical client-relationships sales-strategy crm b2b microsoft-office leadership organization negotiation compliance

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Sr Dir, Business Development

Syneos Health · Full Time · 7 months ago

Syneos Health

🌎 United States 💵 $121K - $266K per year ⭐ 10+ yrs exp 💼 Sales

The Executive Director, Regional BD is responsible for driving sales growth across an assigned geographic territory by balancing proactive expansion of existing accounts with the pursuit of new opportunities. This role involves developing tailored engagement plans and collaborating with cross-functional teams to address client-specific challenges.

salesforce medical client-relationships sales-strategy crm b2b microsoft-office leadership organization negotiation compliance

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Sr Medical Scientist

Syneos Health · Full Time · 8 months ago

Syneos Health

🌎 United States 💵 $79800 - $139K per year ⭐ 5-10 yrs exp 💼 Healthcare

The Sr Medical Scientist works with the Medical Director to develop medical plans and engages with outside experts for necessary medical input. They perform medical reviews, analyze data for risks and trends, and manage project deliverables to meet milestones.

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Sr CRA I - Sponsor dedicated - Chile Home Based

Syneos Health · Full Time · 9 months ago

Syneos Health

🌎 Chile ⭐ 2-5 yrs exp 💼 Others

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with clinical practices. Collaborate with cross-functional teams to support clinical trial activities and ensure successful execution of clinical trials.

medical clinical-research agile communication reporting training documentation organization time-management compliance

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Sr CRA | Sponsor Dedicated | Oncology (Home-Based - Atlanta, GA)

Syneos Health · Full Time · 9 months ago

Syneos Health

🌎 Georgia, United States 💵 $80600 - $145K per year ⭐ 5-10 yrs exp 💼 Others

The Sr CRA is responsible for site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulatory and protocol standards. They will assess site performance, manage site-level activities, and support patient recruitment and retention strategies.

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CRA II (German and French Speaking)

Syneos Health · Full Time · 9 months ago

Syneos Health

🌎 Ukraine ⭐ 2-5 yrs exp 💼 Others

The CRA II is responsible for performing site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulatory and protocol standards. They will also assess site performance and communicate any serious issues to the project team while supporting patient recruitment and retention strategies.

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