Associate Principal Statistical Analyst
Revolution Medicines
Revolution Medicines seeks an Associate Principal Statistical Analyst with 10-14 years of experience in clinical trial programming to oversee statistical programming resources and deliverables for oncology studies. The role involves technical leadership, regulatory compliance, and quality assurance across early and late-phase clinical programs.
Responsibilities
- Provide technical oversight of statistical programming contractors and CROs
- Mentor junior staff and develop future leaders in company values
- Ensure quality and timely delivery of programming analysis datasets and deliverables
- Quality control clinical trial results and regulatory submission documents
- Manage timelines and vendors for submission-related programming activities
Requirements
- 10-14 years of statistical programming experience in biotech or pharma
- BS/BA degree or equivalent qualification in relevant field
- Direct programming experience with early or late-phase clinical trials
- CDISC standards expertise including SDTM, ADaM, and define.xml
- Knowledge of FDA 21 CFR Part 11 and GxP regulatory standards
- Demonstrated ability to multitask and work in interdisciplinary teams
- Preferred: oncology clinical trial experience and strong leadership record
Vacancy posted 28 days ago
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