Jobs at Syneos Health

The Single Sponsor Payment Specialist will assist in site management activities, maintain clinical tracking information, and coordinate supplies for assigned studies, ensuring compliance with protocols and guidelines.

Manage late-phase, single-sponsor clinical trials including CRO/vendor coordination, site evaluations and monitoring, protocol/document drafting, data review and reporting, and training/mentoring junior staff, ensuring regulatory and GCP compliance.

Manage clinical trial sites, ensure compliance with regulations, assess site performance, conduct monitoring visits, and optimize site activities throughout the trial lifecycle.

The Clinical Project Manager II will oversee clinical trials, manage study timelines, ensure compliance with regulations, and coordinate cross-functional teams.

The role involves overseeing clinical trials, creating project plans, managing budgets, ensuring compliance with regulations, and developing recruitment strategies.

Manage interdisciplinary clinical research projects, ensuring compliance with regulations, overseeing project delivery and liaising with clients while driving financial performance and managing project teams.

The Project Manager II coordinates clinical study timelines, collaborates with teams, ensures compliance with regulations, oversees operational aspects of trials, and develops recruitment strategies for successful enrollment.

Manage and coordinate clinical research studies, ensuring compliance with regulations, maintaining study documentation, and facilitating communication among stakeholders.

Lead and deliver statistical activities across clinical trial lifecycle: prepare SAPs, generate randomization schedules, review CRFs and database design, coordinate biostatistics and programming teams, perform QC/verification, support regulatory interactions, mentor staff, and contribute to business development. Minimal travel.

Lead RWD analysis strategy and execution: develop technical specifications and statistical programs, perform complex observational analyses (propensity scoring, ML), validate cohorts/variables, ensure QC, collaborate cross-functionally, and communicate results to non-technical stakeholders.

The Director of Epidemiology Pipeline collaborates on virology clinical trials, providing scientific expertise, leading project proposals, and overseeing study management and regulatory compliance.

Lead and deliver high-complexity pre-award feasibility assessments for global clinical trials across therapeutic areas. Independently analyze site-level data, prepare presentations/reports, support bid defenses, liaise with internal stakeholders, mentor junior staff, and contribute to process and data asset development to support RFPs and feasibility strategy.

The Internal Account Director will lead patient recruitment and retention strategies for clinical trials, ensuring successful enrollment and collaboration with various stakeholders.

The role involves managing clinical research projects, ensuring compliance with regulations, coordinating teams, overseeing budgets, and developing client relationships, while providing leadership and training to staff.

The Principal Biostatistician leads biomarker analysis for clinical studies, develops evaluation plans, conducts data analyses, mentors staff, and ensures accurate statistical deliverables while collaborating across teams.

The role involves site management in clinical trials, including site qualification, monitoring, compliance verification, data accuracy, and communication with site staff to ensure regulatory standards are met.

Responsible for site qualification, management activities, and ensuring compliance with regulations and protocols for clinical studies.

The role involves programming and data review for real-world data analysis, supporting epidemiologists, and managing complex data sets using statistical programming languages and tools.

The Principal Statistician oversees biostatistics projects, mentors staff, prepares statistical plans, and ensures quality and regulatory compliance in clinical trials.

The Manager of Biostatistics oversees biostatisticians, ensuring project quality, adherence to regulations, and managing staff development while meeting financial targets.