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.

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

Qualifications

• 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 revi...