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 essential trial documentation.
Syneos Health
267 Remote Job Openings at Syneos Health
Collaborate with Medical Directors to develop medical plans and perform regular medical review 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.
Clinical Trial Manager with experience working with United States as a CTM - Argentina, Brazil, Chile, Colombia or Mexico Home Based
Syneos Health
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Full Time
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6 hours ago
Syneos Health
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, coordinating with project teams, and ensuring data integrity and patient safety.
Per Diem - Freelance Research Nurse - Lille (France)
Syneos Health
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Full Time
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11 hours ago
Syneos Health
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.
Local Contractor - Research Nurse (per diem) - Lavaveix-Les-Mines area (France)
Syneos Health
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Full Time
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11 hours ago
Syneos Health
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.
Ensures the integrity of revenue recognition policies and sets global reporting standards for actuals, forecasts, and backlog. Supervises a team of finance professionals to support therapeutic areas in achieving financial targets.
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.
eCOA Project Manager with at least 2 years of experience in Clinical Trials & eCOA technologies - Argentina Home Based
Syneos Health
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Full Time
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13 hours ago
Syneos Health
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.
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.
Develop custom SAS code to generate summary tables, listings, and graphs according to statistical analysis plans. Act as the lead statistical programmer by directing activities, reviewing project documentation, and mentoring junior personnel.
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.
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.
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 guidance to site staff and junior CRAs.
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.
Medical Director- Psychiatry (US Based Only - Board-certified in Psychiatry is required)
Syneos Health
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Full Time
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a day ago
Syneos Health
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.
TMF Specialist (Safety processing only) - Min 1 year of previous exp in in central file management - Argentina, 100% home-based
Syneos Health
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Full Time
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a day ago
Syneos Health
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 document owners to resolve discrepancies.
Manager, FSP 360 (Sponsor dedicated) - Sao Paulo, Brazil Home Based
Syneos Health
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Full Time
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a day ago
Syneos Health
The role is responsible for managing multifunctional FSP360 team members and ensuring high-quality service delivery to customers. Key duties include overseeing team performance, managing resource availability, and maintaining compliance with regulatory guidelines and SOPs.
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.
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.
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.
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.
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.
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.
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.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory requirements. Develop monitoring tools and collaborate with cross-functional teams to support clinical trial operations.
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.
Patient Reimbursement Coordinator (Argentina Based)
Syneos Health
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Full Time
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3 days ago
Syneos Health
Manage travel logistics and reimbursement processing for patients participating in clinical trial projects. Coordinate with project managers and clinical sites to ensure timely payments and compliance with study policies.
Payment Specialist - Sponsor-dedicated - Poland
Syneos Health
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Full Time
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3 days ago
Syneos Health
Manage and execute site and participant payments in compliance with Clinical Trial Agreements and regulatory requirements. Coordinate with cross-functional teams to resolve payment issues and maintain accurate financial records in electronic systems.
The role involves supporting clinical monitoring staff with site management and ensuring compliance with protocol requirements. Key tasks include maintaining the Trial Master File, tracking regulatory documents, and coordinating site supplies.
Senior Clinical Trial Manager - FSP (Tagalog proficient)
Syneos Health
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Full Time
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3 days ago
Syneos Health
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 performance of CRAs and Central Monitors.
Country Study Operations Manager (Sponsor Dedicated) Homebased, Turkey
Syneos Health
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Full Time
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3 days ago
Syneos Health
Develop and coordinate Phase 1 clinical research studies while ensuring compliance with regulatory requirements and GCP guidelines. Manage study logistics, resource allocation, and stakeholder communication to ensure project milestones and deliverables are met.
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.
Develop and implement Phase 1 clinical research studies while ensuring adherence to protocols, timelines, and global regulations. Coordinate between investigators, clients, and operations teams to manage logistics, resources, and study progress.
Tijdelijke CRA Nederland - diabetes, obesitas en metabole ziekten
Syneos Health
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Full Time
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6 days ago
Syneos Health
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.
Regulatory Consultant - CMC (CMC with small molecule products)
Syneos Health
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Full Time
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6 days ago
Syneos Health
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.
Sr Programmer-Sr Data Scientist/Analys Real-World Data (SAS/R)
Syneos Health
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Full Time
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6 days ago
Syneos Health
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.
Principal Statistical Programmer (US, CAD, UK only)
Syneos Health
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Full Time
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6 days ago
Syneos Health
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.
Director, Project Delivery (Early Phase/ClinPharm Exp Must Have + Neuroscience Exp - Good to have)
Syneos Health
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Full Time
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6 days ago
Syneos Health
Provides high-level oversight for assigned projects to ensure study launch, conduct, and closeout align with contractual agreements and quality standards. Manages financial aspects, risk mitigation, and senior-level customer relationships while mentoring junior project delivery staff.
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 and contract negotiations.
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.
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.
Feasibility Strategy Analytics Lead (Sponsor dedicated) - Argentina, Brazil and Mexico Home Based
Syneos Health
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Full Time
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7 days ago
Syneos Health
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.
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.
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.
Associate Director/Director Strategy, Real World Evidence and Late Phase
Syneos Health
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Full Time
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7 days ago
Syneos Health
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.
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.
Clinical Trial Manager (Sponsor dedicated) - Experience in project management and previous experience as CRA - Argentina Home Based
Syneos Health
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Full Time
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8 days ago
Syneos Health
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.
Sr Biostatistician (Therapeutic Areas -Oncology / Vaccines)
Syneos Health
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Full Time
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8 days ago
Syneos Health
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.
Principal Biostatistician (Therapeutic Areas - Oncology / Vaccines)
Syneos Health
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Full Time
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8 days ago
Syneos Health
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.
The Sr 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 guidance to site staff and junior CRAs.
Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA)
Syneos Health
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Full Time
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8 days ago
Syneos Health
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.
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 Director (HIV Research Scientific Lead - Clinical/Observational Research)
Syneos Health
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Full Time
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8 days ago
Syneos Health
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.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and oversee investigational product administration.
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.
Medical Writer I (Junior Project Specialist - 1 year Contract)
Syneos Health
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Full Time
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9 days ago
Syneos Health
The role involves managing compliant document filing and eTMF activities within the Veeva RIM system. It also requires maintaining project timelines and collaborating with stakeholders to ensure regulatory standards are met.
Senior Clinical Scientist Clinical Surveillance & Training
Syneos Health
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Full Time
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9 days ago
Syneos Health
The role involves designing and reviewing clinical protocols, managing clinical scales, and providing training on therapeutic indications and scale scoring. It also includes performing clinical and statistical analysis of endpoint data and collaborating with investigators to ensure protocol compliance.
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.
Data Management Specialist - Home Based Bulgaria
Syneos Health
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Full Time
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12 days ago
Syneos Health
The role involves managing complex data processes, including bulk mapping, enrichment, and cleansing to ensure high data quality. Additionally, the specialist coordinates with IT and governance teams while monitoring performance against KPIs.
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.
CRA II - Sponsor Dedicated - Neurology / Oncology (Home-Based in Puerto Rico)
Syneos Health
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Full Time
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12 days ago
Syneos Health
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.
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.
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.
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.
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.
Experienced Clinical Research Associate - Sponsor Dedicated
Syneos Health
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Full Time
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13 days ago
Syneos Health
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.
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.
CRA II or Sr CRA (sponsor dedicated) - Min 3 years of prev exp in monitoring - Santiago, home-based
Syneos Health
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Full Time
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13 days ago
Syneos Health
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.
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred
Syneos Health
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Full Time
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13 days ago
Syneos Health
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.
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.
Serve as the strategic executive leader for large anchor accounts, focusing on profitable growth, operational excellence, and C-suite relationship management. Orchestrate cross-functional teams to deliver high-impact results and execute multi-year account strategies.
Perform comprehensive site management activities including qualification, initiation, and monitoring to ensure regulatory and protocol compliance. Manage clinical data integrity, investigational product accountability, and maintain essential study documentation.
Principal Medical Writer (Regulatory focus) - Sponsor-dedicated - Poland, Belgium, Netherlands, Spain
Syneos Health
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Full Time
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13 days ago
Syneos Health
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.
CRA II/Sr CRA I - Sponsor-dedicated; Poland (Central Poland preferred)
Syneos Health
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Full Time
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14 days ago
Syneos Health
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.
Responsible for leading and managing Site Start-Up (SSU) deliverables to ensure study sites are activation-ready on time and in compliance. This includes overseeing regulatory activities, clinical trial agreements, and essential document collection throughout the study life cycle.
CRA II - Multi Sponsor - Cardiology or Huntington's Therapeutic Experience
Syneos Health
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Full Time
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14 days ago
Syneos Health
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.
CRA I/II - Beijing/Shanghai/Guangzhou/Chengdu/Nanjing/Hangzhou/Tianjin/Changsha/Zhengzhou/Changchun
Syneos Health
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Full Time
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14 days ago
Syneos Health
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.
Clinical Scientist - Clinical Surveillance & Training (Clinical Psychologist/Neuropsychologist - Must Have)
Syneos Health
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Full Time
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14 days ago
Syneos Health
The role focuses on ensuring endpoint quality and data integrity by designing rater training programs and performing patient eligibility reviews. The Clinical Scientist also analyzes clinical data to provide actionable insights and partners with sponsors on protocol strategy.
Principal, Global Feasibility (pre-award strategy) - Sponsor-dedicated - EMEA
Syneos Health
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Full Time
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14 days ago
Syneos Health
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.
Line Manager, FSP 360 – Cairo, Egypt | Travel Required
Syneos Health
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Full Time
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14 days ago
Syneos Health
The role is responsible for managing the performance and daily activities of a multifunctional team to ensure high-quality service delivery and customer satisfaction. It involves direct interaction with customer points of contact to manage KPIs, resource availability, and compliance with SOPs and GCP guidelines.
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.
CRA Germany - multi-sponsor (north-east Germany)
Syneos Health
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Full Time
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15 days ago
Syneos Health
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.
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.
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.
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.
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.
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.
The Senior Project Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements. They act as the primary liaison between the company and customers to manage timelines, budgets, and project deliverables.
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 maintain the Investigator Site File.
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.
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.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and oversee investigational product accountability.
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.
Customer Contract Manager (Budgeting Exp Required)
Syneos Health
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Full Time
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19 days ago
Syneos Health
Owns and manages the end-to-end contract process, focusing on the development and execution of contractual documents and change orders. Collaborates with Pricing and Proposals teams to finalize budgets and negotiate financial terms with customers.
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.
The role involves authoring CMC sections for post-approval variations and managing life cycle activities for the EU and GCC markets. Responsibilities include conducting gap analyses, preparing regulatory submissions, and providing subject matter expertise to multidisciplinary project teams.
Call Center Agent, 6 month contract, must be fluent in French and Italian and residing in France
Syneos Health
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Full Time
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20 days ago
Syneos Health
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.
Assessment Scientist: Masters in Psychology; Psychometrists
Syneos Health
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Full Time
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21 days ago
Syneos Health
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.
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.
Clinical Scientist - Clinical Surveillance & Training (PhD Clinical Psychologist/Neuropsychologist/MD Psychiatrist)
Syneos Health
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Full Time
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21 days ago
Syneos Health
The Clinical Scientist leads rater training excellence and performs comprehensive patient eligibility reviews to ensure data integrity. They analyze clinical endpoint data to provide actionable insights and partner with sponsors to shape protocol strategies.
Sr CRA – Minimum 4 Years of CRA Experience is a Must - Riyadh
Syneos Health
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Full Time
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21 days ago
Syneos Health
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.
IMS Specialist I/II - Clinical Payment Specialist (Sponsor-dedicated) Poland
Syneos Health
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Full Time
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22 days ago
Syneos Health
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.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and provide guidance to site staff and junior CRAs.
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred
Syneos Health
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Full Time
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22 days ago
Syneos Health
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.
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.
Internal Account Director - Recruitment & Retention Strategy
Syneos Health
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Full Time
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22 days ago
Syneos Health
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.
The Project Manager is responsible for overseeing trial master file management, coordinating study deliverables, and managing vendors. They also handle financial reporting, budget reconciliation, and risk mitigation strategies to ensure study milestones are met.
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.
Central Risk Manager (RBQM & Central Monitoring)
Syneos Health
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Full Time
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22 days ago
Syneos Health
Serve as a subject matter expert in RBQM and Centralized Monitoring to develop risk-based strategies and monitoring plans for global clinical trials. Partner with sponsors and cross-functional teams to identify critical risks and leverage data analytics for proactive mitigation.
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.
Sr Site Contract Specialist - Fluent French Required - Sponsor Dedicated
Syneos Health
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Full Time
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23 days ago
Syneos Health
Administers all 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 site-specific contracts.
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.
Site Contracts Specialist II/Sr - Sponsor dedicated
Syneos Health
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Full Time
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23 days ago
Syneos Health
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.
Site Contracts Specialist II/Sr - Sponsor dedicated
Syneos Health
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Full Time
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23 days ago
Syneos Health
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.
Develop and manage monitoring strategies and risk assessments (RACT) to ensure data quality and integrity in clinical trials. Collaborate with cross-functional leads and sponsors to mitigate risks and ensure compliance with ICH/GCP and country regulations.
The Central Risk Manager develops and implements monitoring strategies and risk assessments (RACT) to ensure data quality and integrity. They collaborate with cross-functional leads and sponsors to mitigate risks and ensure compliance with ICH/GCP and country regulations.
Clinical Trial Manager with focus on project management - Sponsor dedicated - Argentina, BA
Syneos Health
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Full Time
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24 days ago
Syneos Health
Oversees site management, clinical monitoring, and data integrity to ensure patient safety and regulatory compliance. Coordinates with functional leaders to meet study milestones and manages the clinical project team's deliverables.
Principal Statistician Oncology with Submission Experience
Syneos Health
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Full Time
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24 days ago
Syneos Health
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.
R Statistical Programmer - Submission Experience Required (hiring in Armenia, UK, India, SA)
Syneos Health
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Full Time
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24 days ago
Syneos Health
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.
Site Contracts Specialist I (Serbia) Sponsor Dedicated
Syneos Health
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Full Time
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24 days ago
Syneos Health
Administers contract management processes, including the coordination of agreements and budgets for clinical trial sites. Collaborates with legal, finance, and clinical operations to ensure timely execution and archival of contracts.
Medical Scientist/Sr Medical Scientist (Hyderabad/Bangalore )
Syneos Health
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Full Time
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a month ago
Syneos Health
The role involves serving as a Clinical Data Reviewer to identify data errors, issue queries, and ensure the medical integrity of study participant data. The scientist will collaborate with sponsors and clinical teams to maintain audit readiness and support data dissemination meetings.
Clinical Trial Manager with focus on Project Management - Sponsor dedicated - Brazil Home Based
Syneos Health
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Full Time
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a month ago
Syneos Health
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.
Local Contractor Research Nurse (Per Diem)- Paris (France)
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
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.
Principal Biostatistician - Biomarker (EMEA Remote)
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
Principal Clinical Trial Regulatory Affairs - +4 years of experience in regulatory submissions in LATAM - Home Based
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
CRA II or Sr CRA (Sponsor dedicated) - Buenos Aires only, home based
Syneos Health
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Full Time
·
a month ago
Syneos Health
The CRA II or Sr CRA is responsible for site qualification, initiation, monitoring, management, and close-out visits, ensuring compliance with regulatory guidelines. They will also assess site performance, manage data integrity, and support subject recruitment and retention strategies.
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.
Senior Project Specialist – Real World Evidence (Sponsor Dedicated /Remote -US Based)
Syneos Health
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Full Time
·
a month ago
Syneos Health
Provide operational and administrative support for Real World Evidence research programs, including both primary and secondary data studies. Coordinate study milestones, manage CTMS tracking, and facilitate communication between epidemiologists, data analysts, and stakeholders.
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.
Administers all 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 site-specific contracts.
Site Contracts Specialist with Clinical Trials experience Home-Based in US
Syneos Health
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Full Time
·
a month ago
Syneos Health
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).
Administers contract management processes and coordinates agreements for clinical trials, including budgets and site-specific contracts. Collaborates with legal, finance, and clinical operations to ensure timely execution and compliance with SOPs.
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.
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.
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 guidance to site staff and junior CRAs.
Sponsor Dedicated Global Senior Project Manager (CTL level role) remote
Syneos Health
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Full Time
·
a month ago
Syneos Health
The Clinical Trial Leader is responsible 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.
Senior CRA - Phase I oncology trials - Hamburg/Berlin region
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
Sr CRA in Oncology - Sponsor Dedicated - Home Based in Hungary
Syneos Health
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Full Time
·
a month ago
Syneos Health
The Sr CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, oversee data integrity, and may provide mentorship to junior CRA staff.
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.
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.
Clinical Trial Manager I/ll. Remote based in Canada
Syneos Health
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Full Time
·
a month ago
Syneos Health
The Clinical Trial Manager serves as the functional lead accountable for site management, clinical monitoring, and central monitoring of assigned studies. They provide leadership and technical support to the Clinical Operations team to ensure compliance with monitoring plans and quality deliverables within budget.
Call Center Agent, 6 month FTC. Fluency in German and English essential
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
Clinical Data Associates– Future Roles (India)
Syneos Health
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Full Time
·
a month ago
Syneos Health
The role involves managing clinical database entries, performing data validation, and resolving queries according to study-specific plans. It also includes conducting quality control checks and assisting in the finalization and transfer of clinical databases to sponsors.
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.
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.
The Financial Analyst II is responsible for analyzing financial data, developing insights, and driving decision support for business stakeholders. Key duties include managing budgeting, forecasting, and producing monthly financial reports and commentary for global management.
The Sr. Site Contracts Specialist will lead multi-country projects, negotiating and preparing contracts and budgets for clinical trials. They will also ensure quality control of contracts and maintain strong relationships with internal and external teams.
Mgr, FSP 360 (Sponsor dedicated) - At least 2 years of experience as a People Manager in CRO or Pharma environment - Sao Paulo, Brazil Home Based
Syneos Health
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Full Time
·
a month ago
Syneos Health
The role involves managing customer delivery and success, ensuring compliance with KPIs, and fostering strong relationships with clients. Additionally, it includes overseeing team performance and supporting professional development.
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.
Sr Programmer Sr Data Scientist/Analyst OMOP (NA & UK Only)
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
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.
Senior Medical Writer (Medical Information Writing)
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
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.
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.
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.
Clinical Scientist - Immunology (Expertise in Ulcerative Colitis, Crohn’s disease and Rheumatology + Excel)
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
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.
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.
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.
Sr RW Programmer/Sr Data Scientist/Analyst - Real World Data(US and UK Only)
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 agreements.
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.
Patient Engagement Lead – Global Clinical Trial Recruitment and Retention
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
Develop custom SAS programming code to generate summary tables, listings, and graphs according to statistical analysis plans. Act as the lead statistical programmer by directing activities of other personnel and ensuring quality standards and regulatory compliance.
Develop custom SAS code to generate summary tables, listings, and graphs while ensuring compliance with statistical analysis plans and regulatory guidelines. Act as a lead statistical programmer by directing activities, reviewing documentation, and serving as a CDISC subject matter expert.
Sr Clinical Operation Specialist / Lead Clinical Operation Specialist (immediate Joiner)
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
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.
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.
Internal Account Director (Recruitment & Retention)
Syneos Health
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Full Time
·
a month ago
Syneos Health
Lead the development and execution of patient recruitment and retention plans for global clinical trials. Act as a strategic advisor in bid defense meetings and collaborate cross-functionally to ensure enrollment targets are met.
CRA SSU - Experience in monitoring and regulatory - Sponsor dedicated - Colombia Home Based
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
Principal Biostatistician(Clinical Pharmacology)
Syneos Health
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Full Time
·
a month ago
Syneos Health
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.
Site Contracts Specialist with CRO/Pharma experience home-based in Serbia
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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.
Associate Director of Real World Evidence (Pharma Co Experience Required) - Remote US
Syneos Health
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Full Time
·
2 months ago
Syneos Health
Develop and execute study protocols, analysis plans, and reports to answer priority research questions using Real World Evidence. Design and manage epidemiological and data science projects to support internal decision-making and regulatory responses.
Lead the design, development, and execution of epidemiological and RWE projects, including study protocols and analysis plans. Communicate research results through regulatory documents, publications, and internal decision-making reports.
Sr Stat/ Pr Stat Programmer (PKPD Programming)
Syneos Health
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Full Time
·
2 months ago
Syneos Health
Develop custom programming code to generate summary tables, listings, and graphs for PKPD analysis according to statistical analysis plans. Act as a lead programmer by directing activities, reviewing project documentation, and mentoring junior personnel.
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.
Clinical Supply Chain Manager ** open to several EMEA countries (Homebased) **
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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.
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.
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.
Sponsor Dedicated CRA II/Sr CRA - Oncology I Home Based Israel
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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 coordinating with global project teams.
Medical Director- Ophthalmology - Board-certified in Ophthalmology is required
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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 and site staff.
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.
Senior CRA België / Belgique - Single Sponsor - Oncology
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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 oversee investigational product accountability.
On-site monitor ** open to diverse EMEA countries **
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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.
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.
West Coast Regional Leader, Business Development
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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.
Stat Programmer II/ Sr Statistical Programmer (R/R Shiny)
Syneos Health
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Full Time
·
2 months ago
Syneos Health
The role involves creating data visualizations using R Shiny and performing data wrangling within the clinical domain. The programmer will manage clinical trial data and potentially lead multiple studies.
Senior Statistical Programmer (Clinical Pharmacology)
Syneos Health
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Full Time
·
2 months ago
Syneos Health
Develop custom programming code using SAS to generate summary tables, listings, and graphs while ensuring quality standards and regulatory compliance. Act as a lead statistical programmer to direct programming activities, mentor personnel, and represent the team in sponsor meetings.
Pr. Statistical Programmer (Clinical Pharmacology)
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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.
Sr Medical Writer, Redaction (Clinical Trial Transparency)
Syneos Health
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Full Time
·
2 months ago
Syneos Health
The Senior Medical Writer is responsible for authoring, quality assurance, and editing clinical study documents for regulatory submissions. They also perform systematic quality control checks and provide mentorship to team members to ensure project timelines and standards are met.
Clinical Assessment Scientist - COA Lead - Sponsor-dedicated (Sweden, Spain, UK, South Africa, Portugal, Denmark)
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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.
The specialist maintains safety and pharmacovigilance documentation, ensures regulatory compliance, and supports audit readiness. They also manage safety databases, track quality metrics, and assist in the development of proposals and training materials.
Sr Clinical Technology Specialist, Trial Informatics - Sr COS. Spain. FSP
Syneos Health
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Full Time
·
2 months ago
Syneos Health
The Senior Analyst supports the administration and technical oversight of Veeva Clinical systems to ensure data accuracy and standardized metric collection. They collaborate with study teams and IT to manage system enhancements, user access, and integration functionality to optimize clinical trial activities.
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.
Sr. CRA I (Sponsor dedicated) - Sao Paulo, Brazil Home Based
Syneos Health
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Full Time
·
2 months ago
Syneos Health
The Senior CRA I performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
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.
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.
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.
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.
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.
Senior Medical Editor. FSP Spain. Must have previous clinical editing exp.
Syneos Health
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Full Time
·
2 months ago
Syneos Health
The Senior Medical Editor is responsible for the quality control, editing, and formatting of nonclinical and clinical documents to ensure compliance with submission standards. This role also involves managing document publishing tasks and overseeing editorial workflows to meet project timelines.
Sr. Medical Editor (Regulatory Documents + QC) - US Home based
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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.
Single Sponsor Senior Medical Editor - Must have previous clinical editing exp.
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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.
CTM II - Sponsor dedicated - Argentina Home Based
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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.
Experienced Clinical Research Associate - Full-Service- West Coast
Syneos Health
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Full Time
·
2 months ago
Syneos Health
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
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.
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.
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.
CRA II Germany - eastern Germany (Leipzig, Halle, Dresden)
Syneos Health
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Full Time
·
2 months ago
Syneos Health
The CRA II is responsible for performing 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 maintain essential study documentation.
The Medical Director provides medical oversight for clinical studies, acting as the primary medical contact and ensuring subject safety. They also contribute to protocol design, pharmacovigilance, and provide therapeutic training to project teams.
CRA II/Sr CRA I - Sweden, Sponsor-dedicated (Pipeline REQ)
Syneos Health
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Full Time
·
2 months ago
Syneos Health
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.
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.
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.
The Senior Medical Writer leads the preparation of complex regulatory documents, ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-functional reviews and provide mentorship to less experienced team members.
Site Care Partner I (SrCRA) - FSP, Sponsor Dedicated
Syneos Health
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Full Time
·
3 months ago
Syneos Health
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.
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.
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.
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.
R Statistical Programmer (hiring in Armenia, Hungary, Estonia, CR, Romania, Argentina, Brazil, or Columbia only)
Syneos Health
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Full Time
·
3 months ago
Syneos Health
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.
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.
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.
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.
Clinical Ops Specialist - Future roles (Bulgaria)
Syneos Health
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Full Time
·
3 months ago
Syneos Health
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.
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.
Executive Director, Strategic Business Development
Syneos Health
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Full Time
·
3 months ago
Syneos Health
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.
The role is within a fully integrated biopharmaceutical solutions organization focused on accelerating customer success by translating clinical, medical affairs, and commercial insights into outcomes. Employees are expected to take initiative and challenge the status quo in a competitive and ever-changing environment.
CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec)
Syneos Health
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Full Time
·
3 months ago
Syneos Health
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.
CRA II (Multi-sponsor) - Ophtalmology experience is required - Brazil Home Based
Syneos Health
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Full Time
·
3 months ago
Syneos Health
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.
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.
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.
Safety & PV Coordinator II (Data Validation) - Based in Sofia Area
Syneos Health
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Full Time
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3 months ago
Syneos Health
The role involves supporting safety, pharmacovigilance, and regulatory operations, including data validation and ensuring compliance with guidelines. Key tasks include reviewing data, identifying discrepancies, and maintaining structured data.
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.
Experienced Clinical Trial Manager - Full-Service
Syneos Health
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Full Time
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4 months ago
Syneos Health
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.
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.
Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; US/CAN
Syneos Health
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4 months ago
Syneos Health
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.
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.
Head of R&D and Scientific Strategy, Rare Disease
Syneos Health
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Full Time
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4 months ago
Syneos Health
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.
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.
CRA SSU with at least 2 years of regulatory experience - Sponsor dedicated - Argentina Client Based
Syneos Health
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Full Time
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4 months ago
Syneos Health
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.
Principal Biostatistician (Rshiny - EMEA BASED)
Syneos Health
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Full Time
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5 months ago
Syneos Health
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.
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Montreal, Quebec, Canada)
Syneos Health
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Full Time
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5 months ago
Syneos Health
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.
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.
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.
Principal Medical Scientist (Project Lead) - RWE - Poland, Bulgaria, Romania, Spain, UK - Sponsor-dedicated
Syneos Health
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Full Time
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5 months ago
Syneos Health
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.
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.
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.
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.
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.
Senior Medical Writer (Scientific Writing +Veeva)
Syneos Health
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Full Time
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6 months ago
Syneos Health
The Senior Medical Writer will mentor less experienced writers and manage medical writing activities for individual studies. They will develop various documents and ensure adherence to regulatory standards while coordinating with different departments.
Medical Writer II (Clinical Trial Transparency)
Syneos Health
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Full Time
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6 months ago
Syneos Health
The Medical Writer II will compile, write, and edit medical writing deliverables with minimal supervision, while also mentoring less experienced writers. Responsibilities include developing clinical documents and ensuring adherence to regulatory standards.
Senior Medical Writer (Abstracts, Manuscripts)
Syneos Health
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Full Time
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6 months ago
Syneos Health
The Senior Medical Writer leads writing projects and mentors less experienced writers. They manage medical writing activities, develop various documents, and ensure adherence to regulatory standards.
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.
Sr CRA I - Sponsor dedicated - Chile Home Based
Syneos Health
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Full Time
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7 months ago
Syneos Health
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.
Director, Safety and PV - Technology, Innovation & AI Enablement
Syneos Health
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Full Time
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7 months ago
Syneos Health
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.
Sr Principal Communication/ Publication Strategy - Single Sponsor
Syneos Health
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Full Time
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8 months ago
Syneos Health
Leads the completion of complex medical writing deliverables and manages medical writing activities associated with individual studies. Advises clients on data presentation strategies and coordinates quality reviews to ensure high standards are maintained.
Sr CRA | Sponsor Dedicated | Oncology (Home-Based - Atlanta, GA)
Syneos Health
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Full Time
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8 months ago
Syneos Health
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.
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.