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Posted 4 hours ago
Associate Director, Biostatistics
Revolution MedicinesAssociate Director, Biostatistics – Early Phase
Requirements
Ph.D. or M.S. in Statistics/Biostatistics, 5-8 years biotech/pharma experience, Oncology trial design experience, Proficiency in SAS or R
Skills
BiostatisticsOncologySASR
About the role
Responsibilities
- Serve as a study level statistician for oncology studies
- Represent biostatistics on study and project teams
- Provide statistical expertise for design, analysis, and reporting of clinical studies
- Collaborate on study design, protocol development, and statistical methodology
- Develop statistical analysis plans and analysis specifications
- Partner with statistical programming to ensure analysis follows specifications
- Collaborate with data management and clinical operations for robust data collection
- Provide statistical input for regulatory interactions and health authority submissions
- Assist in data interpretation and ensure accuracy in publications
- Contribute to functional-level standards, SOPs, and templates
Requirements
- Ph.D. in Statistics/Biostatistics with 5+ years of experience or M.S. with 8+ years of experience
- Experience in biotech/pharma industry as a statistician for clinical trials
- Hands-on experience in design and analysis of oncology trials
- Proficiency in SAS and/or R
- Ability to apply advanced statistical methods like Bayesian methods or predictive modeling
- Strong verbal and written communication skills
- Excellent interpersonal and project management skills
About the Company
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins.
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Get started — it's freeAssociate Director, Biostatistics
Revolution Medicines · Redwood City
