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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 role involves programming in SAS for statistical analysis, managing projects, documentation, and ensuring compliance with regulatory standards in clinical trials.

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.

The Pr. Clinical Programmer leads technical support and application administration of clinical programming tools. Responsibilities include software development, documentation, monitoring application performance, project coordination, and mentoring junior staff, while ensuring quality deliverables across multiple studies.