Tech Stack

Description

As a new member of the Revolution Medicines team, you will lead statistical efforts for European access strategies, regulatory submissions, and healthcare technology assessments, supporting the development of novel targeted therapies for RAS-addicted cancers. You will collaborate with cross-functional teams to design and execute statistical analyses for value dossiers and ensure alignment with European regulatory and market access needs.

Requirements

• PhD or MS in Statistics/Biostatistics with 10+ years (PhD) or 15+ years (MS) industry experience
• Solid knowledge of ICH and regulatory requirements for biostatistics
• Proficiency in SAS or R
• Excellent communication and project management skills

Responsibilities

• Provide statistical leadership for EU access strategies and regulatory submissions
• Design and oversee statistical analyses for value dossiers including ITC and NMA
• Support EU regulatory interactions (EMA Scientific Advice, MAA, Type II variations)
• Contribute to global statistical strategy for approval and reimbursement
• Drive department initiatives and best practices