Associate Director, Clinical Data Management

Scorpion Therapeutics; California (MO); On-site; USD 186,000 - 233,000; Full time

Job summary

Revolution Medicines is seeking an Associate Director, Clinical Data Management to lead data activities across all trial phases for oncology programs focused on RAS mutations. You will oversee data collection, accuracy, and vendor oversight, while ensuring adherence to Data Management Plans and protocols.

The role requires extensive experience in clinical trials, FDA/ICH/GCP knowledge, and leadership of both external vendors and internal teams, with onsite work in California.

Qualifications

• MS/BS degree required.
• 11+ years' experience in designing and executing clinical trials.
• Strong knowledge of clinical databases, medical coding, GCP, FDA, ICH regulations.

Responsibilities

• Oversee data activities across all trial phases for oncology programs.
• Ensure data collection, accuracy and completeness; manage data timelines.
• Coordinate with external vendors and internal teams; review protocols and CRFs.
• Manage EDC database administration and adherence to Data Management Plans.

Skills

Clinical trial design

Data management

Vendor oversight

Regulatory knowledge (FDA/ICH)

EDC database management

Leadership

Education

MS/BS degree

Tools

EDC systems

Job description

Role: Associate Director, Clinical Data Management at Revolution Medicines, overseeing clinical trial data activities across all phases for oncology trials targeting RAS mutations.

Responsibilities include managing data collection, ensuring data accuracy and completeness, vendor oversight, review of protocols and CRFs, EDC database management, and adherence to Data Management Plans. The role involves cross-functional collaboration, leadership of external vendors and internal teams, and project management of data timelines.

Requirements: MS/BS degree, 11+ years' experience in designing and executing clinical trials, strong knowledge of clinical databases, medical coding, GCP, FDA, ICH regulations, with industry experience essential. Preferred: oncology experience, especially in solid tumors, and 5+ years of line management.

High-value: oncology, RAS inhibitors in clinical development, focus on trial data integrity and vendor coordination.

Work setup: onsite in Redwood City, CA, salary range $186K - $233K, with focus on leadership, compliance, and technical expertise.