Jobs at Syneos Health

Lead statistical programming for clinical trials using SAS and R to produce ADaM/SDTM datasets, TLFs, and derived outputs. Validate and QC code, maintain inspection-ready documentation, manage multiple projects, mentor junior programmers, participate in sponsor meetings, and ensure compliance with SOPs and regulatory guidelines. Minimal travel may be required.

The role requires a Senior Statistical Programmer with expertise in R and R Shiny to create visualizations and work with clinical trial data, alongside managing multiple studies and effective communication.

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.

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

The Safety and PV Ops Specialist II maintains compliance with safety regulations, supports quality assurance activities, and manages safety database operations while ensuring training and proposal support for the Pharmacovigilance 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.

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 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.

The Clinical Scientist in Clinical Surveillance & Training will ensure endpoint quality and data integrity in clinical trials, lead training programs, analyze data for insights, and collaborate with various teams to enhance study execution and outcomes.

The Principal Clinical Programmer develops statistical programming solutions, supports data visualization, and leads clinical programming projects, utilizing advanced programming skills and collaborating with clinical teams.

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.