Jobs at Syneos Health

The Project Specialist at Syneos Health will collaborate on biopharmaceutical projects, support customer success, and contribute to clinical development initiatives within a diverse team.

Lead biostatistics activities across clinical trial lifecycle for oncology/vaccine studies. Mentor and supervise biostatisticians, develop and review SAPs, generate randomization schedules, review CRFs and database design, create programming specifications, and represent biostatistics on project teams to ensure high-quality statistical deliverables.

Lead statistical activities across clinical study lifecycle: develop SAPs and mock tables, review CSR and CRFs, coordinate biostatistics and programming, perform QC, create analysis datasets and randomization schedules, and represent biostatistics on project teams for oncology/vaccine studies.

Lead project-level non-CRF data management: define non-CRF data types, coordinate vendors and transfers, implement IXRS UAT, manage DTS/DTA/FFS and testing, ensure data delivery, oversee TMF and financials, report to sponsors, mentor staff, and maintain SOP compliance.

Lead statistical programmer using SAS to develop tables, listings, figures, and derived datasets per SAP and specifications. Validate outputs, maintain documentation, ensure regulatory compliance, mentor and direct other programmers, participate in sponsor meetings, manage multiple projects and timelines, and support inspection readiness. Minimal travel possible.

Provide regulatory expertise to support drug development and commercialization, advise on regulatory strategy and compliance, collaborate with clients and cross-functional teams to shape solutions across clinical programs.

The Safety & PV Specialist I is responsible for data entry and tracking of safety reports, maintaining compliance with SOPs, and conducting literature reviews related to safety in clinical trials.

The Sr. Statistical Programmer develops programming code using SAS to generate statistical outputs, ensures quality standards, manages multiple projects, and leads programming teams. Responsibilities include documentation, communication with teams, and mentoring programming personnel while participating in sponsor meetings.

Provide senior biostatistical support for clinical development programs: design analyses, collaborate with cross-functional teams, oversee statistical methods and reporting, and contribute to regulatory submissions and study interpretation.

The Senior HRIS Analyst manages Workday applications, drives HRIS projects, supports system optimization, and enhances user experience. They train staff, ensure data integrity, analyze needs for improvements, and collaborate with global teams.

The Principal Biostatistician in Clinical Pharmacology will lead statistical aspects of clinical studies, contribute to research design, and collaborate with teams to ensure drug development success.

Execute central report review activities to ensure patient safety, protocol/GCP/regulatory compliance, and data integrity. Review site and central monitoring documentation, document revisions and approvals in CTMS, identify and escalate serious issues, record observations and protocol deviations for action, assess report quality and trends, and participate in project meetings and training.

The Clinical Scientific Advisor supports clinical trial activities, builds relationships with KOLs, and ensures protocol execution. Requires 2+ years in clinical research, preferably in Neuroscience/Psychiatry.

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.

Develop and validate SAS programs to produce SDTM, ADaM, and TLF outputs per SAP/specs; ensure QC, documentation, and inspection readiness. Lead and mentor programmers, participate in sponsor meetings, provide CDISC/DEFINE.XML guidance, support ISS/ISE and safety/efficacy analyses, and contribute to SOPs and tooling. Minimal travel.