Senior Director, Clinical Data Management

Revolution Medicines

Redwood City, United States
Base: $244,000—$305,000 usd; bonus/equity: not spe...
On-site
Data integrity and regulatory compliance
Lead and manage data management teams
Oversee departmental budgets
Revolution Medicines is seeking a Senior Director of Clinical Data Management to lead their data management functions in clinical research focused on oncology. The ideal candidate will have extensive experience in clinical data management, leadership skills, and a deep understanding of regulatory requirements and clinical trial methodologies

Job Summary

  • The Senior Director of Clinical Data Management provides high-level leadership for data management functions within clinical research, focusing on strategic development, operational execution, and regulatory compliance to ensure data integrity for clinical trials.
  • Key responsibilities include leading and managing data management teams, establishing and enforcing data management policies and procedures, overseeing departmental budgets, collaborating with cross-functional teams and vendors, and ensuring data management processes meet regulatory standards.
  • This role requires extensive experience in clinical data management, strong leadership and communication skills, expertise in clinical trial methodologies, and a deep understanding of regulatory requirements including submissions and data management systems.

Matching Summary

Match Score: 85

Revolution Medicines is seeking a Senior Director of Clinical Data Management to lead their data management functions in clinical research focused on oncology. The ideal candidate will have extensive experience in clinical data management, leadership skills, and a deep understanding of regulatory requirements and clinical trial methodologies.

Salary

Base: $244,000—$305,000 USD; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Data integrity and regulatory compliance
  • Lead and manage data management teams
  • Oversee departmental budgets
  • Collaborate with cross-functional teams
  • Manage CRO and vendor relationships
  • Ensure data quality and compliance with GCPs

Nice-to-have

  • Exposure to real-world data
  • Decentralized trial models
  • Automation and digital transformation

Key Requirements

  • 17+ years of experience in clinical data management
  • Experience in oncology therapeutic area
  • Proficient knowledge of EDC systems (e.g., Medidata Rave)
  • Proficient knowledge of CDISC standards
  • Experience with global trials and regulatory submissions (FDA, EMA)
  • BS/BA degree or suitable qualification

Work Rights

Not specified

Tailored Resume

Cover Letter