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
✔ ImmunologyTA experience – good to have, not mandatory
✔ R programming knowledge – desirable but not required