Associate Director, Statistical Programming
Full-time
Revolution Medicines
Revolution Medicines seeks an Associate Director of Statistical Programming with 14+ years of oncology clinical trial experience. The role involves hands-on SAS programming, team oversight, and regulatory submission support for early and late-phase studies.
Responsibilities
- Collaborate with cross-functional teams to establish programming timelines and deliverables
- Provide SAS programming technical guidance and support to team members
- Oversee regulatory submissions including CDISC-compliant datasets and documentation
- Lead programming support for early or late-phase studies as needed
- Manage vendor timelines and conduct verification reviews of study documents
Requirements
- 14+ years statistical programming experience in oncology clinical trials
- Bachelor's degree or equivalent qualification in relevant field
- Leadership experience with programming contractors and vendors
- Proficient in SAS for analysis datasets, tables, listings, and figures
- Strong multitasking and cross-functional collaboration abilities
- Knowledge of CDISC standards and regulatory requirements (FDA 21 CFR Part 11)
Vacancy posted 1 day ago
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