Jobs at Syneos Health

Manage single-sponsor oncology clinical studies end-to-end: lead project teams, ensure GCP/regulatory compliance, oversee budgets and TMF, coordinate vendors, support inspection readiness, and deliver client reporting while mitigating risks.

Provide administrative and logistical support for clinical trial supplies under the Clinical Trial Supplies Manager or Project Lead: assist distribution, resupply and return planning, support batch manufacturing and packaging record review, customs clearance, and inventory forecasting in collaboration with project teams and vendors.

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 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.

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

The CRA II/Senior CRA will perform site management activities, ensure compliance with regulations, conduct monitoring visits, and support recruitment efforts throughout the clinical trial process.

The Principal Biostatistician oversees statistical tasks, mentors staff, prepares analyses, and ensures high-quality deliverables throughout project lifecycle.

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

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

The R Statistical Programmer prepares custom programming code using R, validates outputs, adheres to regulatory guidelines, leads programming activities, mentors colleagues, and ensures timely delivery of project deliverables.

Oversee biostatistical activities, mentor staff, prepare statistical plans, ensure quality control, and manage multiple clinical projects while interfacing with regulatory agencies.

The Executive Assistant provides high-level administrative support to the Business Unit Head, managing calendars, travel, communications, and preparing executive presentations. Skills needed include organization, discretion, and strong communication.

Ensure effective clinical research operations, monitor study progress, adhere to regulations, and coordinate communication with clinical trial participants.

Performs on-site and remote site qualification, initiation, monitoring and close-out visits to ensure ICH-GCP/GPP and protocol compliance. Verifies informed consent, source data vs CRF, manages IP and ISF/TMF reconciliation, documents monitoring activities, supports recruitment and audit readiness, and collaborates with sponsors and site staff. May perform chart abstraction and train junior staff in real-world late-phase studies.