Senior Director, Clinical Data Management
Revolution Medicines
Location
Redwood City, CA
Job Type
Full-time
Posted
June 16, 2026
Views
21
Salary Range
$244k - $305k
USD
Job Description
Revolution Medicines seeks a senior leader for clinical data management in their oncology division. The role focuses on strategic oversight, team leadership, and regulatory compliance for RAS-targeted cancer therapies currently in clinical development.
Key Responsibilities
- Establish vision, strategy, and departmental procedures for clinical data management
- Lead and develop data management teams with resource planning and performance oversight
- Establish KPIs for data quality and operational metrics
- Manage CRO and vendor partnerships to ensure quality standards
- Oversee departmental budgets and expenditures
- Ensure regulatory compliance with FDA, ICH, and GCP requirements
- Guide data management for regulatory submissions and inspections
- Collaborate cross-functionally with clinical, quality, and regulatory teams
- Drive innovation through new technologies and process improvements
Required Qualifications
- 17+ years direct clinical data management experience in biotech or pharma
- MS, BS/BA degree or equivalent qualification in relevant field
- Leadership experience in oncology therapeutic area
- Proficiency with EDC systems (e.g., Medidata Rave) and CDISC standards
- Experience with global trials and FDA/EMA regulatory submissions
- Knowledge of medical dictionary coding and industry standards
- Strong team leadership and motivational abilities
Preferred Qualifications
- Degree in life sciences, health informatics, or related field
- Exposure to real-world data and decentralized trial models
- Experience with automation and digital transformation (IXRS, AI/ML, RBQM)
Compensation: $244,000 - $305,000 USD. Work arrangement: Hybrid (Redwood City, CA headquarters).
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Frequently Asked Questions
Where is the job located, and what is the work-mode policy?
The position is based in Redwood City, CA, and operates under a hybrid work arrangement.
What are the required qualifications and experience level for this role?
Candidates need 17+ years of direct clinical data management experience in biotech or pharma, a BS/BA, MS, or equivalent degree, and leadership experience in oncology. Proficiency with EDC systems (like Medidata Rave), CDISC standards, global trials, FDA/EMA regulatory submissions, and medical dictionary coding is also required.
What are the key responsibilities of the Senior Director?
You will establish clinical data management vision and strategy, lead and develop teams, set KPIs, and manage CRO and vendor partnerships. Additionally, you will oversee budgets, ensure regulatory compliance (FDA, ICH, GCP), guide regulatory submissions, collaborate cross-functionally, and drive technological innovation.
What is the salary range for this position?
The compensation range for this role is $244,000 - $305,000 USD.
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Job Information
Source:
manual
AI Relevance:
30/100
(Somewhat related)
Remote Type:
hybrid
Experience:
Director
Allowed Locations:
Worldwide
Skills & Tags:
clinical data management
EDC
CDISC
Medidata Rave
oncology
regulatory submissions
AI/ML
RBQM
real-world data
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