Description
As a Principal Biostatistician, you will provide end-to-end statistical leadership and integration support across Phase II and Phase III studies, working closely with cross-functional stakeholders in a fast-paced, global environment.
Key Responsibilities
- Provide Principal-level Biostatistics support for Phase II–III clinical trials
- Independently lead SAP authoring and review
- Support integration activities across studies and programs
- Act as a proactive statistical partner to Clinical, Programming, and Regulatory teams
- Ensure delivery of high-quality, compliant statistical outputs within timelines
- Communicate clearly and confidently with internal and external stakeholders
Candidate Requirements
- Strong experience as a Principal Biostatistician (Pharma or CRO)
- End-to-end knowledge of Phase II and III studies
- Proven expertise in SAP writing and reviewing
- Ability to work independently with minimal supervision
- Proactive, solution-oriented communicator
- Immunology TA experience – good to have, not mandatory
- Strong R Programming experience