Principal Statistician
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Job Description
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The contractor will provide statistical expertise and operational support for oncology clinical trial projects, with responsibility for ensuring the accuracy, quality, and reproducibility of statistical deliverables. The role requires strong oncology clinical trial experience, working knowledge of CDISC standards, and the ability to collaborate effectively with internal study teams and relevant functional partners, as applicable.
Key Responsibilities
- Support statistical analyses of oncology endpoints, including time-to-event and response-based endpoints.
- Perform event projections to estimate the timing of planned event-driven analyses.
- Review and provide feedback on SDTM and ADaM specifications, tables, listings, figures, statistical analysis plans, protocol amendments, and relevant study documentation.
- Conduct routine study data review to identify inconsistencies, missing data, or other issues that may affect analysis or interpretation.
- Validate statistical outputs and provide documentation supporting reproducibility and quality control.
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ClinChoice
View Company ProfileClinChoice is a leading global Clinical Research Organization (CRO) dedicated to accelerating the development and commercialization of innovative drugs, medical devices, and diagnostics. Founded in 1995 and headquartered in Horsham, Pennsylvania, the company operates with a massive global footprint, boasting over 3,000 clinical experts across the Americas, Europe, and Asia. Under the hood, ClinChoice delivers end-to-end full-service and Functional Service Provider (FSP) solutions—spanning clinical operations, biometrics, regulatory affairs, and post-marketing safety. Their primary target audience includes emerging and mid-sized biotech startups, as well as top-tier global pharmaceutical giants (partnering with 6 of the top 10 pharma companies globally). What sets ClinChoice apart in the highly regulated life sciences sector is its deep therapeutic expertise and tech-enabled delivery model, having successfully supported over 3,000 clinical studies and 10,000 regulatory submissions worldwide to bring life-saving treatments to market faster.
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