Revolution Medicines · 7 hours ago
Associate Director, Clinical Data Management
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies for RAS-addicted cancers. The Associate Director of Clinical Data Management will manage clinical trial data, collaborate with functional leaders, and oversee data management tasks to ensure the success of clinical trials.
Health CareLife ScienceMedical
Responsibilities
Manage day-to-day activities of Clinical Data Management (CDM) for clinical trials
Define project-level data management strategy
Identify requirements for capturing and processing clinical data ensuring accuracy, consistency, and completeness
Manage external vendors providing clinical data
Perform data management tasks including SAE reconciliation and query management
Provide CDM oversight of outsourced clinical trials
Plan, coordinate, and manage CDM tasks for clinical studies
Participate and review CRO proposals
Act as primary liaison with CROs and third-party data vendors
Review clinical protocols and cross-functional plans
Serve as primary reviewer or author of case report forms (CRFs)
Oversee EDC database development, testing, maintenance, and lock/unlock
Ensure Data Management Plans are followed throughout studies
Set and manage Data Management project timelines
Provide comprehensive status updates to project team members
Address data issues identified by cross-functional team members
Assist in defining and creating data listings and summary table validation
Implement data standardization and maintain data model across projects
Direct management and mentoring responsibilities for internal data management team members
Lead department initiatives e.g., development of SOPs
Other duties as assigned
Qualification
Required
MS, BS/BA with 12+ years of related experience or other suitable qualification with relevance to the field
Direct experience of designing and running early-stage clinical trials
Knowledge of, and experience with databases, standards, medical terminology, medical coding dictionaries, quality control processes, and auditing procedures
Good working knowledge of ICH, FDA, and GCP regulations and guidelines
A demonstrable record of strong leadership and teamwork
Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment
Excellent written and verbal communication skills
Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute on goals as a member of an interdisciplinary team is extremely important
Preferred
Experience working within the biotechnology or pharmaceutical industry
Deep experience supporting oncology clinical trials, including hands‑on involvement with the operational and data‑related complexities unique to oncology studies
Benefits
Competitive cash compensation
Robust equity awards
Strong benefits
Significant learning and development opportunities
Company
Revolution Medicines
Revolution Medicines is an innovative and dynamic organization of expert biologists, chemists, pharmacologists, clinical scientists.
H1B Sponsorship
Revolution Medicines has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (13)
2024 (18)
2023 (15)
2022 (8)
2021 (1)
2020 (2)
Funding
Current Stage
Public CompanyTotal Funding
$2.25BKey Investors
Royalty PharmaBoxer CapitalNextech Invest
2025-06-24Post Ipo Debt· $250M
2024-12-02Post Ipo Equity· $750M
2023-03-02Post Ipo Equity· $323.6M
Recent News
Pharmaceutical Technology
2026-01-13
Company data provided by crunchbase