Syneos Health

Principal Medical Writer

Syneos Health · Full Time · an hour 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.

medical agile feedback documentation organization literature compliance

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Principal Medical Writer

Syneos Health · Full Time · an hour 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.

medical agile feedback documentation organization literature compliance

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

Syneos Health · Full Time · 13 hours 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 · 15 hours 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.

medical agile documentation organization compliance

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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 · 15 hours 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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Site Activation Specialist I/II - Shanghai or Nanjing

Syneos Health · Full Time · a day ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Responsible for managing site activation and regulatory submissions at the country level to ensure timely trial start-up. This includes coordinating with ethics committees, regulatory authorities, and managing site contracts and budgets.

agile communication training organization compliance

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Regulatory Specialist - Germany

Syneos Health · Full Time · a day ago

Syneos Health

🌎 Germany ⭐ 5-10 yrs exp 💼 Legal

The role involves managing regulatory pathways and site start-up deliverables for clinical trials, ensuring compliance with internal and customer expectations. Key duties include preparing submission documents, managing project budgets, and overseeing the life cycle maintenance of regulatory activities.

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FSP- CRA II/ SCRA

Syneos Health · Full Time · a day ago

Syneos Health

🌎 New Zealand ⭐ 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.

medical document-review agile communication training science organization compliance

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Associate Dir, Proposals/RFIs

Syneos Health · Full Time · a day 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 · a day 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.

medical agile training organization compliance

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Proposal Writer

Syneos Health · Full Time · 2 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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Director, Epidemiology RWE (Onco or Immunology)

Syneos Health · Full Time · 2 days ago

Syneos Health

🌎 United States 💵 $118K - $207K per year ⭐ 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. This includes developing study protocols, analysis plans, and communicating results through regulatory documents and scientific publications.

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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 · 2 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 · 2 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.

medical agile documentation organization compliance

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Principal Clinical Trial Regulatory Affairs - +4 years of experience in regulatory submissions in LATAM - Argentina, Mexico or Brazil Home Based

Syneos Health · Full Time · 2 days ago

Syneos Health

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

Acts as a Regulatory Subject Matter Expert to lead site activation pathways and manage regulatory submissions for clinical trials in LATAM. Responsibilities include line management of staff, developing strategic client relationships, and ensuring project deliverables meet quality and budget expectations.

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Senior Project Specialist (Sponsor Dedicated) Austria/Germany

Syneos Health · Full Time · 2 days ago

Syneos Health

🌎 Austria ⭐ 2-5 yrs exp 💼 Product

The role involves setting up and maintaining project files, including TMF and regulatory documents, across various databases. It also requires providing administrative support to project leads and coordinating communication between team members and site staff.

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

Syneos Health · Full Time · 2 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 · 2 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 · 2 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 · 2 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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CRA in Oncology - Sponsor dedicated - Part Time 0.3 FTE - Fixed term contract - Home Based in Hungary

Syneos Health · Full Time · 2 days ago

Syneos Health

🌎 Hungary ⭐ 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

Syneos Health · Full Time · 2 days ago

Syneos Health

🌎 Germany ⭐ 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 accuracy, and maintaining the Trial Master File.

medical document-review agile communication training science organization compliance

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CRA II

Syneos Health · Full Time · 2 days ago

Syneos Health

🌎 Taiwan ⭐ 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.

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Sr.CRA II for FSP BU

Syneos Health · Full Time · 2 days ago

Syneos Health

🌎 South Korea ⭐ 5-10 yrs exp 💼 Others

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

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Senior Medical Editor. Spain. FSP

Syneos Health · Full Time · 5 days ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Writing

Responsible for the quality control review, copyediting, and formatting of clinical documents for submission to global health authorities. This includes verifying data against source tables and overseeing the workload and schedules for other editors.

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Dir, Compensation Infrastructure & Analytics

Syneos Health · Full Time · 5 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.

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Senior Site Contracts Lead

Syneos Health · Full Time · 5 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.

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Project Data Management (Data Acquisition Specialist-Non-CRF)

Syneos Health · Full Time · 5 days ago

Syneos Health

🌎 India ⭐ 10+ yrs exp 💼 Data Entry

Responsible for the project management of non-CRF data management services, acting as the functional lead and primary contact for internal and external stakeholders. This includes managing vendor transfer agreements, overseeing data collection deliverables, and ensuring all milestones meet contractual and regulatory requirements.

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PCS Project Manager

Syneos Health · Full Time · 5 days 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.

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Independent Contractor Research Nurse - Munich Germany

Syneos Health · Full Time · 5 days 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.

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

Syneos Health · Full Time · 5 days 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.

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

Syneos Health · Full Time · 5 days 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.

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Clinical Data Reviewer - Oncology Required (US, CAN Only)

Syneos Health · Full Time · 6 days ago

Syneos Health

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

Perform clinical review of participant-level data to ensure readiness for milestones such as interim analysis and submissions. Identify data inconsistencies, generate queries, and collaborate with study teams to resolve discrepancies from a clinical perspective.

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Medical Writer - MLR Technical Reviewer / Scientific Expert - FSP in Spain. Portuguese/French Proficiency

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Spain ⭐ 2-5 yrs exp 💼 Writing

Perform quality checks on scientific and medical assets to ensure accuracy and regulatory compliance. Manage reference tagging and claims object creation within the Veeva Vault platform.

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Sr.Stat programmer clin pharm

Syneos Health · Full Time · 6 days 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.

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Site Activation Specialist II - Min 2 years of regulatory experience in Mexico - 100% Remote role

Syneos Health · Full Time · 6 days ago

Syneos Health

🌎 Mexico ⭐ 2-5 yrs exp 💼 Legal

Responsible for managing country-level site activation deliverables, including regulatory submissions to Ethics Committees and Competent Authorities. The role involves overseeing the end-to-end site activation process and providing subject matter expertise on local regulatory intelligence in Mexico.

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Independent Contractor Research Nurse - Munich, Germany

Syneos Health · Full Time · 7 days 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.

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CRA II FSP

Syneos Health · Full Time · 7 days ago

Syneos Health

🌎 Argentina ⭐ 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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Regulatory Senior Consultant

Syneos Health · Full Time · 7 days 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.

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Customer Contract Manager (Budgeting Exp Required)

Syneos Health · Full Time · 8 days ago

Syneos Health

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

Owns and manages the end-to-end contract process, focusing on the development and execution of contractual documents to ensure customer satisfaction. Collaborates with Pricing and Proposals teams to finalize budgets and negotiate financial terms with customers.

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CRA II - Sponsor-dedicated (Poland)

Syneos Health · Full Time · 8 days 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.

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

Syneos Health · Full Time · 8 days 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.

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

Syneos Health · Full Time · 8 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 accuracy, and maintain the Investigator Site File.

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Sr CRA I - Changsha

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 China ⭐ 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 integrity, and maintain the Investigator Site File and Trial Master File.

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Sr Statistical Programmer(ADaM & TLF)

Syneos Health · Full Time · 8 days ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Software Development

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

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Medical Writer I - Clinical Trial Transparency Specialist - Poland (Sponsor-dedicated)

Syneos Health · Full Time · 9 days ago

Syneos Health

🌎 Poland ⭐ 2-5 yrs exp 💼 Writing

Manage the anonymization of datasets and documents to ensure compliance with regulatory requirements and GDPR guidance. Collaborate with Biostatistics and Regulatory Operations to publish redacted clinical trial documents for Health Canada, EMA, and ClinicalTrials.gov.

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CRA II - Sponsor-dedicated - only Central Poland

Syneos Health · Full Time · 9 days 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 performance, verify clinical data integrity, and maintain essential trial documentation.

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CRAI

Syneos Health · Full Time · 9 days ago

Syneos Health

🌎 China ⭐ 0-2 yrs exp 💼 Others

The CRA I 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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CRA I - Guangzhou

Syneos Health · Full Time · 9 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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Sr Sales Incentive Compensation & Financial Analyst

Syneos Health · Full Time · 11 days ago

Syneos Health

🌎 India ⭐ 2-5 yrs exp 💼 Sales

The role manages the end-to-end administration of sales incentive compensation and commission programs, ensuring data accuracy and resolving inquiries. It involves partnering with Sales Operations and Business Development to perform commission calculations and provide analytical support for leadership decision-making.

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

Syneos Health · Full Time · 11 days 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).

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

Syneos Health · Full Time · 12 days 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.

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Safety & PV Specialist I - Mexico Remote

Syneos Health · Full Time · 12 days 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.

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

Syneos Health · Full Time · 12 days 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.

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CRA II/Sr CRA I - Sponsor-dedicated; Poland

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Poland ⭐ 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.

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CRA II - Chengdu

Syneos Health · Full Time · 12 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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FSP- CRAII (Melb/ Sydney/ Brisbane)

Syneos Health · Full Time · 12 days ago

Syneos Health

🌎 Australia ⭐ 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.

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Clinical Data Associate III / Sr CDA (FSP) - Min 2 years of previous data management exp - Argentina, home-based

Syneos Health · Full Time · 13 days ago

Syneos Health

🌎 Argentina, Colombia ⭐ 2-5 yrs exp 💼 Data Entry

The role involves managing clinical trial data, performing User Acceptance Testing (UAT), and ensuring data consistency across various databases. It also includes coordinating other Clinical Data Associates and supporting the Project Data Manager in updating study documentation.

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

Syneos Health · Full Time · 13 days 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.

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CRA II, Multisponsor ** Remote PORTUGAL **

Syneos Health · Full Time · 13 days ago

Syneos Health

🌎 Portugal ⭐ 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.

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CRA II/Sr CRA - Single Sponsor

Syneos Health · Full Time · 13 days ago

Syneos Health

🌎 Poland ⭐ 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 CDA (Data Acquisition Specialist-Non-CRF)

Syneos Health · Full Time · 13 days ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Others

Lead Clinical Data Associates in the collection and management of Non-CRF data across multiple global clinical trials. Oversee study set-up, conduct, and closeout activities while serving as a backup for the Project Data Manager.

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CRA II or Sr CRA (Multi-sponsor) - Brazil Home Based

Syneos Health · Full Time · 14 days ago

Syneos Health

🌎 Brazil ⭐ 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

Clinical Country & Site Associate (Clinical Trial Manager) - Sponsor dedicated - Sao Paulo, Brazil Home Based

Syneos Health · Full Time · 14 days ago

Syneos Health

🌎 Brazil ⭐ 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

Site Contracts Specialist (Polish Required)

Syneos Health · Full Time · 14 days 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.

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Regulatory Consultant

Syneos Health · Full Time · 14 days 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.

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CRA II/Snr CRA

Syneos Health · Full Time · 14 days 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.

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CRA II/ SCRA I

Syneos Health · Full Time · 14 days 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.

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CRA II/ SCRA

Syneos Health · Full Time · 14 days 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

Senior Site Contracts Specialist (Sponsor Dedicated /Remote – U.S. Only) Clinical Trial Contracts experience required!

Syneos Health · Full Time · 14 days ago

Syneos Health

🌎 Spain 💵 $56400 - $95900 per year ⭐ 2-5 yrs exp 💼 Healthcare

Independently manage and negotiate Clinical Trial Agreements (CTAs) and budgets for research sites in the U.S. and Canada. Collaborate with cross-functional teams to ensure efficient study activation and maintain accurate documentation within tracking systems.

APPLY

Clinical Country & Site Associate (Clinical Trial Manager)

Syneos Health · Full Time · 15 days 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 accuracy, and maintain the Investigator Site File and Trial Master File.

APPLY

CRA II- SCRA I

Syneos Health · Full Time · 15 days 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

Regulatory Associate - AdPromo

Syneos Health · Full Time · 15 days ago

Syneos Health

🌎 Argentina, Brazil, Mexico ⭐ 2-5 yrs exp 💼 Legal

The role involves building and institutionalizing regulatory project management frameworks and tools to enhance GRA-AP capability. It also requires providing oversight of projects and portfolios to ensure alignment with objectives and timelines.

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Central Report Reviewer

Syneos Health · Full Time · 16 days 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.

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Sample Management Specialist - Experience with end-to-end sample management process - Argentina Home Based

Syneos Health · Full Time · 16 days ago

Syneos Health

🌎 Argentina ⭐ 0-2 yrs exp 💼 Others

The role involves managing the end-to-end process of study samples, including receipt, inventory, storage, and disposition. It also requires maintaining storage equipment and ensuring the integrity of reference materials and reagents.

APPLY

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

Syneos Health · Full Time · 16 days 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

Sponsor Dedicated Global Senior Project Manager (CTL level role) remote

Syneos Health · Full Time · 16 days ago

Syneos Health

🌎 Austria, Germany ⭐ 10+ yrs exp 💼 Product

The Clinical Trial Leader is accountable for the set-up, execution, and delivery of assigned trials within the Evidence Network. They provide leadership and direction to the trial team to ensure efficient execution and value for subjects and sites.

APPLY

Sr.CRA II - Warsaw

Syneos Health · Full Time · 16 days 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 · 19 days 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 · 19 days 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 · 19 days 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 · 19 days 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 · 20 days 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

Sr. Clinical Programmer

Syneos Health · Full Time · 20 days ago

Syneos Health

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

Design, write, and validate software and documentation for clinical programming projects using tools like Medidata Rave and SAS. Lead development activities across multiple concurrent studies while providing technical support and senior review for high-quality deliverables.

APPLY

Senior/ Principal Statistical Programmer (R/RShiny)

Syneos Health · Full Time · 20 days 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 · 20 days 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 · 21 days 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 · 21 days 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 · 21 days 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

Clinical Research Associate (CRA) Germany

Syneos Health · Full Time · 21 days 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

CRA Real World Late Phase - Germany

Syneos Health · Full Time · 21 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, data integrity, and subject safety for Real World Late Phase studies.

APPLY

Sr Project Manager - Beijing/Shanghai

Syneos Health · Full Time · 21 days ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Product

The role involves managing the Trial Master File (TMF) and coordinating study deliverables across internal departments and vendors. It also includes overseeing vendor performance, resource management, and assisting with study closure activities.

APPLY

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

Syneos Health · Full Time · 21 days 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 · 22 days 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 · 22 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.

APPLY

Pr Statistical Programmer(ADAM, TLF, SDTM)

Syneos Health · Full Time · 22 days 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

CRA II - Multi Sponsor

Syneos Health · Full Time · 22 days ago

Syneos Health

🌎 United Kingdom ⭐ 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.

APPLY

Medical Writer- Future Roles (India)

Syneos Health · Full Time · 22 days 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

Medical Writer II/ Sr Medical Writer

Syneos Health · Full Time · 24 days ago

Syneos Health

🌎 Germany 💵 $70100 - $145K per year ⭐ 2-5 yrs exp 💼 Writing

Leads the creation and coordination of clinical and regulatory documents, ensuring scientific accuracy and adherence to regulatory standards. Acts as the primary technical contact for internal teams and clients while mentoring junior medical writers.

APPLY

Tijdelijke CRA Nederland - diabetes, obesitas en metabole ziekten

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Netherlands ⭐ 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 performance, verify clinical data integrity, and oversee the handling of investigational products.

APPLY

Regulatory Consultant - CMC (CMC with small molecule products)

Syneos Health · Full Time · a month 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

Sr Programmer-Sr Data Scientist/Analys Real-World Data (SAS/R)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Spain 💵 $80600 - $175K per year ⭐ 5-10 yrs exp 💼 Software Development

Conduct longitudinal cohort studies and perform data analysis including the programming of TFLs. Review protocols and Statistical Analysis Plans (SAP) while assessing the quality of real-world data.

APPLY

Principal Statistical Programmer (US, CAD, UK only)

Syneos Health · Full Time · a month 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 · a month 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 · a month 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 · a month 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

Regulatory Labeling Manager

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Argentina, Colombia, Mexico ⭐ 2-5 yrs exp 💼 Legal

Responsible for developing and maintaining labeling content for mature pharmaceutical products, including CCDSs, USPI, and SmPC. The role involves collaborating with cross-functional teams to ensure regulatory compliance and documenting labeling decisions through governance processes.

APPLY

Clinical Research Associate - Canada

Syneos Health · Full Time · a month 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

Associate Director/Director Strategy, Real World Evidence and Late Phase

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Canada ⭐ 5-10 yrs exp 💼 Others

Act as a subject matter expert in Real World Evidence (RWE) study design and strategy to develop innovative RWD-based solutions. Drive business growth by identifying sales opportunities, managing client relationships, and leading proposal defenses.

APPLY

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

Principal Biostatistician (Therapeutic Areas - Oncology / Vaccines)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 India ⭐ 10+ yrs exp 💼 Healthcare

The Principal Biostatistician serves as a departmental resource, mentoring staff and overseeing the preparation of Statistical Analysis Plans and Clinical Study Reports. They lead the statistical aspects of protocols and ensure high-quality data capture and analysis throughout the project lifecycle.

APPLY

Sr Biostatistician (Therapeutic Areas -Oncology / Vaccines)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Healthcare

Provide statistical support throughout the project lifecycle, from protocol development to the Clinical Study Report. Coordinate biostatistics and programming personnel to ensure high-quality deliverables and maintain project timelines.

APPLY

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

Syneos Health · Full Time · a month 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

Sr.CRA II - FSP - Istanbul or Ankara (Open)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Turkey ⭐ 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 integrity, and maintain the Investigator Site File.

APPLY

Medical Director (HIV Research Scientific Lead - Clinical/Observational Research)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Netherlands 💵 $146K - $277K per year ⭐ 10+ yrs exp 💼 Healthcare

Provides medical oversight and monitoring for clinical studies, including protocol design and development. Acts as the primary medical contact for customers and ensures subject safety and data integrity.

APPLY

CRA II - FSP - Istanbul or Ankara

Syneos Health · Full Time · a month 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

Clin Ops Specialist - Shanghai

Syneos Health · Full Time · a month ago

Syneos Health

🌎 China ⭐ 0-2 yrs exp 💼 Others

The role involves supporting clinical monitoring staff with site management and ensuring compliance with study protocols and guidelines. Key tasks include maintaining the Trial Master File, tracking regulatory documents, and coordinating site supplies.

APPLY

Project Financial Analyst II

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Spain 💵 $56400 - $95900 per year ⭐ 0-2 yrs exp 💼 Finance

Supports the Business Unit Controller in recording monthly revenue, managing project budgets in Oracle, and performing variance analysis. Monitors project health, including gross profit and receivables, while attending project review meetings to ensure forecast accuracy.

APPLY

CRA II - Sponsor Dedicated - Neurology / Oncology (Home-Based in Puerto Rico)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 United States ⭐ 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

Site Activation Manager assigned to Client

Syneos Health · Full Time · a month 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 · a month 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

Project Manager II - Beijing/Shanghai

Syneos Health · Full Time · a month ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Product

Lead interdisciplinary clinical research studies ensuring compliance with GCP 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

Experienced Clinical Research Associate - Sponsor Dedicated

Syneos Health · Full Time · a month 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

Clinical Research Associate - Full-Service

Syneos Health · Full Time · a month 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

Central Monitor II - Remote Mexico

Syneos Health · Full Time · a month 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

Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred

Syneos Health · Full Time · a month ago

Syneos Health

🌎 United States 💵 $95000 - $210K per year ⭐ 5-10 yrs exp 💼 Legal

Responsible for developing high-quality clinical regulatory documents for global submissions, including ISE, ISS, and Clinical Overviews. Provides strategic direction to cross-functional teams and mentors junior medical writers to ensure scientific rigor and regulatory compliance.

APPLY

Sr CRA II (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

Principal Medical Writer (Regulatory focus) - Sponsor-dedicated - Poland, Belgium, Netherlands, Spain

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Belgium, Netherlands, Poland, Spain ⭐ 5-10 yrs exp 💼 Legal

Responsible for developing high-quality clinical documents for global regulatory submissions, including IBs and CSRs. Provides strategic direction to cross-functional teams and mentors junior medical writers to ensure scientific rigor and timely delivery.

APPLY

CRA II - Multi Sponsor - Cardiology or Huntington's Therapeutic Experience

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Poland ⭐ 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 and Trial Master File.

APPLY

Principal, Global Feasibility (pre-award strategy) - Sponsor-dedicated - EMEA

Syneos Health · Full Time · a month ago

Syneos Health

🌎 France ⭐ 5-10 yrs exp 💼 Teaching

Lead high-complexity RFPs and global feasibility assessments across various therapeutic areas to support pre-award strategies. Collaborate with internal stakeholders and clients to deliver data-driven reports and presentations for bid defenses.

APPLY

CRA I Germany

Syneos Health · Full Time · a month 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 · a month 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 Austria

Syneos Health · Full Time · a month 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 Germany - multisponsor

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

Manager FSP 360

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Germany ⭐ 5-10 yrs exp 💼 Others

Manage Clinical Research Associates in Germany and Austria, ensuring delivery and compliance with agreed-upon KPIs and SOPs. Foster strong customer relationships and oversee team performance, headcount management, and professional development.

APPLY

Sr Biostatistician

Syneos Health · Full Time · a month ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Healthcare

The role involves applying deep expertise in biostatistics to support drug development and commercialization for life sciences customers. The candidate will collaborate with cross-functional teams to deliver data-driven solutions that accelerate patient progress.

APPLY

CRA II - SR CRA Brazil

Syneos Health · Full Time · a month 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

Managing Director

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Germany, Lithuania, United Kingdom ⭐ 10+ yrs exp 💼 Others

The Managing Director serves as the strategic leader for large anchor accounts, focusing on profitable growth, operational excellence, and customer satisfaction. They act as an executive relationship holder, influencing C-suite leadership and orchestrating cross-functional teams to deliver high-impact results.

APPLY

CRA II ( Delhi - NCR)

Syneos Health · Full Time · a month ago

Syneos Health

🌎 India ⭐ 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 smooth clinical trial operations.

APPLY

Employee Wellness Specialist

Syneos Health · Full Time · a month 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 · 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 smooth clinical trial operations.

APPLY

Call Center Agent, 6 month contract, must be fluent in French and Italian and residing in France

Syneos Health · Full Time · a month ago

Syneos Health

🌎 France ⭐ 0-2 yrs exp 💼 Support

The agent will assist potential clinical trial participants by conducting pre-screening interviews and guiding them through the eligibility process. Responsibilities include managing travel and reimbursement inquiries and accurately recording patient data in internal systems.

APPLY

Assessment Scientist: Masters in Psychology; Psychometrists

Syneos Health · Full Time · a month 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

Principal Medical Writer. Spain. FSP. Remote.

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Belgium, Poland, Spain ⭐ 5-10 yrs exp 💼 Writing

Responsible for developing high-quality clinical documents for global regulatory submissions, including IBs and CSRs. Provides strategic direction to cross-functional teams and mentors junior medical writers to ensure scientific rigor and timely delivery.

APPLY

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

Syneos Health · Full Time · a month 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

IMS Specialist I/II - Clinical Payment Specialist (Sponsor-dedicated) Poland

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Poland ⭐ 2-5 yrs exp 💼 Finance

The specialist manages investigator payments using CTMS tools and coordinates with internal teams to ensure accurate funding and distribution. They are also responsible for reconciling project grant trackers and reviewing Clinical Trial Agreements to ensure payment terms are met.

APPLY

Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred

Syneos Health · Full Time · a month ago

Syneos Health

🌎 United States 💵 $95000 - $210K per year ⭐ 10+ yrs exp 💼 Legal

Develop global regulatory submission documents including Clinical Study Reports and Clinical Overviews in accordance with ICH guidelines. Manage medical writing projects by developing timelines and coordinating with cross-functional teams to meet corporate objectives.

APPLY

Sr Statistical Programmer (NA Only)

Syneos Health · Full Time · a month 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 · a month 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

Tijdelijke CRA positie Nederland

Syneos Health · Full Time · a month ago

Syneos Health

🌎 Netherlands ⭐ 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 staff, verifying clinical data integrity, and maintaining the Investigator Site File.

APPLY

Manager, Biostatistics

Syneos Health · Full Time · a month 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 · a month ago

Syneos Health

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

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

APPLY

Site Contracts Specialist II/Sr - Sponsor dedicated

Syneos Health · Full Time · a month 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 · a month 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 · a month 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

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

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Brazil ⭐ 5-10 yrs exp 💼 Product

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

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

CST (eCOA) Project Manager (Serbia)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Serbia ⭐ 5-10 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 managing system builds, coordinating with vendors, and collaborating with internal stakeholders to ensure data integrity and protocol objectives are met.

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

Principal Clinical Trial Regulatory Affairs - +4 years of experience in regulatory submissions in LATAM - Home Based

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Colombia ⭐ 5-10 yrs exp 💼 Legal

Acts as a Regulatory Subject Matter Expert to manage clinical trial submissions and site activation pathways, specifically within the LATAM region. Responsible for developing regulatory strategies, managing project budgets, and overseeing the preparation of core dossiers and amendments.

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

Site Contracts Specialist with Clinical Trials experience Home-Based in US

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Healthcare

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 the accurate execution and archival of Clinical Trial Agreements (CTAs).

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

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

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Germany ⭐ 5-10 yrs exp 💼 Others

The Senior CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They manage site-level activities, verify clinical data integrity, and oversee investigational product accountability for oncology trials.

APPLY

Principal Statistical Programmer(ADAM & TLF)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 India ⭐ 10+ yrs exp 💼 Software Development

Develop and maintain statistical programming standards while providing technical leadership for the creation of statistical programs. Collaborate with stakeholders to ensure data integrity and mentor junior programmers to improve overall process quality.

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

Call Center Agent, 6 month FTC. Fluency in German and English essential

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Argentina, India, Serbia ⭐ 0-2 yrs exp 💼 Support

Engage with potential clinical trial participants to conduct pre-screening and determine eligibility. Provide support to randomized patients regarding reimbursement and travel inquiries through triage calls.

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

Sr Programmer Sr Data Scientist/Analyst OMOP (NA & UK Only)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Spain ⭐ 5-10 yrs exp 💼 Software Development

Collaborate with researchers to implement OHDSI/DARWIN compatible solutions and execute OMOP CDM cohorts and analyses. Develop reproducible, production-grade analytics using R, SQL, and AI-enabled workflows while maintaining rigorous documentation.

APPLY

Sr CRA - Sponsor Dedicated - Belgium

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Belgium ⭐ 5-10 yrs exp 💼 Others

The Sr CRA will perform site qualification, initiation, monitoring, management, and close-out visits, ensuring compliance with regulatory standards. They will assess site performance, communicate issues, and support subject recruitment and retention strategies.

APPLY

Senior Medical Writer (Medical Information Writing)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Writing

Lead and manage medical information writing projects, including the creation of global standard scientific response communications and FAQs. Mentor junior writers and collaborate with cross-functional teams to ensure scientific accuracy and regulatory compliance of deliverables.

APPLY

Clinical Scientist - Respiratory

Syneos Health · Full Time · 2 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 - Immunology (Expertise in Ulcerative Colitis, Crohn’s disease and Rheumatology + Excel)

Syneos Health · Full Time · 2 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 - Oncology

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Spain ⭐ 2-5 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 · 2 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 - Ophthalmology

Syneos Health · Full Time · 2 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 - Cardiovascular

Syneos Health · Full Time · 2 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 · 2 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

Account Development Manager

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Singapore ⭐ 2-5 yrs exp 💼 Others

The Account Development Manager is responsible for identifying, engaging, and qualifying prospective biopharmaceutical customers through high-volume outbound outreach. They serve as the link between Marketing and Sales by vetting leads and transitioning them to the Business Development team.

APPLY

Study Manager - Cardiovascular

Syneos Health · Full Time · 2 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 - Respiratory

Syneos Health · Full Time · 2 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 - Ophthalmology

Syneos Health · Full Time · 2 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 - Immunology

Syneos Health · Full Time · 2 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 - Vaccine

Syneos Health · Full Time · 2 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

Study Manager - Oncology

Syneos Health · Full Time · 2 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

Site Activation Specialist I/II - Guangzhou

Syneos Health · Full Time · 2 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

Site Activation Specialist I/II - Beijing

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Responsible for managing site activation and regulatory submissions at the country level to ensure timely trial start-up. This includes coordinating with ethics committees, managing essential documents, and negotiating site contracts and budgets.

APPLY

Patient Engagement Lead – Global Clinical Trial Recruitment and Retention

Syneos Health · Full Time · 2 months ago

Syneos Health

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

The Patient Engagement Lead owns the end-to-end global patient recruitment and retention strategy for clinical trials. This includes managing vendor performance, overseeing Participant Engagement Plans, and serving as the primary strategic contact for sponsors.

APPLY

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

Syneos Health · Full Time · 2 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 · 2 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

CRA SSU - Experience in monitoring and regulatory - Sponsor dedicated - Colombia Home Based

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Colombia ⭐ 2-5 yrs exp 💼 Legal

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

APPLY

Principal Biostatistician(Clinical Pharmacology)

Syneos Health · Full Time · 2 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 · 2 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

Sr CRA FSP Sponsor Dedicated

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Turkey ⭐ 5-10 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 manage site-level activities, verify clinical data integrity, and provide mentorship to junior CRA staff.

APPLY

Clinical Supply Chain Manager ** open to several EMEA countries (Homebased) **

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Bulgaria, Greece, Serbia, Slovakia, United States ⭐ 5-10 yrs exp 💼 Healthcare

Lead the operational and financial management of clinical trial supplies throughout the project life cycle. This includes managing vendors, ensuring GMP/GCP compliance, and overseeing drug distribution plans.

APPLY

SSUS II

Syneos Health · Full Time · 2 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 · 2 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 · 2 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 · 2 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.

APPLY

Research Nurse, Townsville, Australia

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 Australia ⭐ 2-5 yrs exp 💼 Healthcare

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

APPLY

West Coast Regional Leader, Business Development

Syneos Health · Full Time · 2 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.

APPLY

Pr. Statistical Programmer (Clinical Pharmacology)

Syneos Health · Full Time · 2 months ago

Syneos Health

🌎 India ⭐ 5-10 yrs exp 💼 Software Development

The Principal Statistical Programmer develops custom code to generate clinical trial outputs and ensures compliance with statistical analysis plans and regulatory standards. They also act as a technical lead, directing programming activities, mentoring staff, and providing expertise on CDISC standards.

APPLY

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.

APPLY

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.

APPLY

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.

APPLY

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.

APPLY

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.

APPLY

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.

APPLY

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.

APPLY

Sr. Medical Editor (Regulatory Documents + QC) - US Home based

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 United States 💵 $62000 - $108K per year ⭐ 5-10 yrs exp 💼 Legal

The Senior Medical Editor is responsible for performing quality control reviews of complex regulatory documents and ensuring compliance with FDA and EU guidelines. They also serve as a project lead, providing technical support, mentoring staff, and managing editorial timelines and budgets.

APPLY

Single Sponsor Senior Medical Editor - Must have previous clinical editing exp.

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Belgium, Ireland, Spain, Switzerland, United States ⭐ 5-10 yrs exp 💼 Writing

The Senior Medical Editor performs quality control reviews, copy editing, and proofreading of clinical documents for global health authority submissions. They also oversee editor workloads, establish schedules, and coordinate with cross-functional authors.

APPLY

CTM II - Sponsor dedicated - Argentina Home Based

Syneos Health · Full Time · 3 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.

APPLY

Principal Site Grant Manager

Syneos Health · Full Time · 3 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.

APPLY

Clinical Trial Manager

Syneos Health · Full Time · 3 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.

APPLY

CRA Switzerland

Syneos Health · Full Time · 3 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.

APPLY

CRA II/Sr CRA I - Sweden, Sponsor-dedicated (Pipeline REQ)

Syneos Health · Full Time · 3 months ago

Syneos Health

🌎 Denmark, Sweden ⭐ 5-10 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 support subject recruitment and retention strategies.

APPLY

CRA oncology Germany

Syneos Health · Full Time · 3 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.

APPLY

Experimented CRA France - single sponsor

Syneos Health · Full Time · 3 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.

APPLY

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

Syneos Health · Full Time · 3 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.

APPLY

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.

APPLY

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.

APPLY

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.

APPLY

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.

APPLY

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.

APPLY

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.

APPLY

Project Manager - Future roles (Bulgaria)

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Bulgaria ⭐ 2-5 yrs exp 💼 Product

Responsibilities include creating and maintaining the Trial Master File Plan, ensuring quality and inspection readiness, and coordinating study deliverables across functional departments and vendors. The role also involves developing contingency planning, creating metric reports, assisting with financial performance tracking, and facilitating team training.

APPLY

Clinical Ops Specialist - Future roles (Bulgaria)

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Bulgaria ⭐ 2-5 yrs exp 💼 Healthcare

The specialist will be proficient in assigned clinical systems, responding to customer support inquiries, developing knowledge from past issues, and participating in new projects involving system requirements and validation. They will also run routine reports, handle ad hoc requests, and deliver prompt user support by investigating and resolving data discrepancies and issues.

APPLY

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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Executive Director, Strategic Business Development

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Spain ⭐ 10+ yrs exp 💼 Sales

The Executive Director will lead the client engagement strategy, identifying key stakeholders to ensure the successful closure of integrated product offerings, and will work with solution architects to develop bespoke offerings tailored to client needs. This role involves analyzing industry activity, developing annual business plans for market segments, and proactively building a strong pipeline of work.

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

Syneos Health · Full Time · 4 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 · 4 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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Sr CTM (Clinical trial medical Advisors)

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 India ⭐ 2-5 yrs exp 💼 Healthcare

The role involves engaging with Principal Investigators and Sub-Investigators to provide scientific support for assigned clinical studies, reinforcing critical-to-quality protocol elements and troubleshooting site-level scientific implementation barriers. Key duties also include capturing and synthesizing structured investigator insights regarding protocol feasibility and challenges to inform the development team's decision-making.

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Clinical Trial Manager II

Syneos Health · Full Time · 4 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 · 4 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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Experienced Clinical Trial Manager - Full-Service

Syneos Health · Full Time · 4 months ago

Syneos Health

🌎 Spain, United States 💵 $114K - $210K per year ⭐ 5-10 yrs exp 💼 Healthcare

The role is responsible for site management oversight, clinical monitoring, and central monitoring deliverables, focusing on patient safety, compliance, and data integrity across site interactions from activation through closeout. This includes identifying risks, reviewing study scope and budget, escalating issues to the project manager, and ensuring quality of monitoring documentation.

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IMS Specialist I

Syneos Health · Full Time · 4 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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Head of R&D and Scientific Strategy, Rare Disease

Syneos Health · Full Time · 5 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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Sr Dir, Business Development

Syneos Health · Full Time · 5 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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CRA single-sponsor in Germany

Syneos Health · Full Time · 5 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 · 5 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 · 5 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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CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Montreal, Quebec, Canada)

Syneos Health · Full Time · 6 months ago

Syneos Health

🌎 Canada ⭐ 2-5 yrs exp 💼 Others

The CRA II/Sr CRA is responsible for site qualification, initiation, monitoring, management, and close-out visits, ensuring compliance with regulatory and protocol standards. They also assess site performance, communicate issues, and support patient recruitment and retention strategies.

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HR Business Delivery Advisor

Syneos Health · Full Time · 6 months ago

Syneos Health

🌎 France ⭐ 2-5 yrs exp 💼 Recruitment

The role manages and resolves complex Tier 3 HR inquiries, providing guidance on performance and engagement to foster a positive work environment. Core duties include delivering employee relations services, handling performance management, conducting investigations, and supporting talent initiatives like organizational restructurings.

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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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Principal Medical Scientist (Project Lead) - RWE - Poland, Bulgaria, Romania, Spain, UK - Sponsor-dedicated

Syneos Health · Full Time · 6 months ago

Syneos Health

🌎 Bulgaria, Oman, Poland, Romania, Spain, United Kingdom ⭐ 5-10 yrs exp 💼 Product

The Principal Medical Scientist manages project scope, objectives, and quality of deliverables while serving as the primary interface between internal teams, customers, and vendors. They also provide scientific oversight and contribute to the planning and development of medical monitoring and scientific services activities.

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Senior Site Contracts Lead

Syneos Health · Full Time · 6 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 · 6 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.

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Sr Dir, Business Development

Syneos Health · Full Time · 6 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.

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Safety & PV Specialist I - Wuhan

Syneos Health · Full Time · 6 months ago

Syneos Health

🌎 China ⭐ 0-2 yrs exp 💼 Others

The Safety & PV Specialist I is responsible for entering information into quality and tracking systems, processing ICSRs, and maintaining safety tracking for assigned activities. They will also assist in generating timely reports and ensure compliance with regulatory requirements.

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Sr Medical Scientist

Syneos Health · Full Time · 7 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 · 8 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.

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Director, Safety and PV - Technology, Innovation & AI Enablement

Syneos Health · Full Time · 8 months ago

Syneos Health

🌎 Worldwide ⭐ 10+ yrs exp 💼 Software Development

The Director will build, deliver, and scale technology-enabled Safety/Pharmacovigilance solutions for internal operations and customers. This role involves leading cross-functional teams, managing vendor relationships, and representing the organization as a thought leader in PV technology.

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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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