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As a Senior Biostatistician, you will collaborate in a dynamic environment on statistical analysis for clinical trials, contributing to the development of therapies for patients.

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 and support statistical activities across clinical trial lifecycles: prepare SAPs, review CRFs and database design, coordinate biostatistics and programming work, perform QC, support regulatory interactions, mentor staff, and contribute to proposals and study reporting.

The Principal Statistical Programmer develops and maintains programming standards, collaborates with stakeholders, ensures data integrity, mentors junior programmers, and implements efficient programming solutions.

The Senior/Principal Statistical Programmer develops programming code for statistical analysis, ensures output quality, manages project documentation, and leads programming activities while mentoring junior staff.

The Statistical Programmer II will leverage expertise in SAS, R, SQL, and Spotfire for clinical data management and visualization, overseeing multiple studies in the drug development process.

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.

The Senior Statistical Programmer develops SAS code for statistical outputs, ensures quality compliance, manages projects, mentors junior staff, and participates in meetings with sponsors.

Provide statistical support for clinical trials, prepare analysis plans, review programming specifications, coordinate biostatistics activities, and manage project deliverables.

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.