revolutionmedicines
Associate Director, Clinical Data Management
At a Glance
- Location
- Redwood City, California, United States
- Work Regime
- hybrid
- Posted
- 2026-07-21T13:52:48-04:00
Key Requirements
Required Skills
Domain Knowledge
- Clinical
- Education
- Energy
- Finance
- Medical
Requirements
11 or more years’ direct experience of designing and running early-stage or late-stage clinical trials.
Knowledge of, and experience with, clinical databases, standards, medical terminology, medical coding dictionaries, quality control processes, and auditing procedures.
Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment.
Oncology experience, especially in solid tumors.
5 or more years’ direct line management experience.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone.
Responsibilities
This position has a key role in the day-to-day management of Clinical Data Management (CDM) activities.
Including timely and professional management of clinical trial data for all relevant phases.
Represents Revolution Medicines (RevMed) CDM in Clinical Team meetings.
The Associate Director, Clinical Data Management, will be required to collaborate closely with other functional leaders to ensure clinical trial success.
Defines project-level data management strategy.
Identifies requirements for capturing and processing of clinical data ensuring accuracy, consistency, and completeness.