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 reviewing
* Ability to work independently with minimal supervision
* Proactive, solution-oriented communicator
* Neuroscience TA experience – good to have, not mandatory
* R programming knowledge – desirable but not required
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