Description

As a Sr. Clinical Program Manager at Revolution Medicines, you will lead clinical study teams to execute and manage oncology trials, ensuring compliance with GCP and regulatory guidelines. You'll partner cross-functionally to manage timelines, budgets, vendors, and data quality, while also coaching team members and contributing to strategic initiatives.

Requirements

• BS/MS in biological sciences or health-related field
• 10+ years direct Clinical Operations experience in pharma/biotech
• 6+ years cross-functional study management or leadership experience
• Strong knowledge of FDA Regulations, ICH Guidelines, and GCP
• Oncology trials experience

Responsibilities

• Adhere to Clinical SOPs, GCP, and ICH Guidelines
• Lead and manage all aspects of clinical trials within timelines and budgets
• Partner with cross-functional teams to manage project timelines, budgets, and data reviews
• Conduct risk management, contingency, and scenario planning
• Supervise project status, communicate issues, and solve problems to meet goals