Revolution Medicines · 10 hours ago
Associate Director, Clinical Data Management
San Francisco Bay Area
Full-time
Onsite
Lead/Staff, Director/Executive
$186K/yr - $233K/yr
12+ years expRevolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies for RAS-addicted cancers. The Associate Director, Clinical Data Management will manage the day-to-day activities of clinical trial data management, collaborate with functional leaders, and ensure the accuracy and completeness of clinical data.
Health CareLife ScienceMedical
Responsibilities
Plans, coordinates, and manages CDM tasks for clinical studies
Participate and review CRO proposals
Acts as primary liaison with CROs, third party data vendors, EDC vendors
Reviews clinical protocols and cross functional plans
Serves as primary reviewer or author of case report forms (CRFs) and CRF completion guidelines
Oversees and participates in all aspects of EDC database development, testing, maintenance, and lock/unlock
Ensures Data Management Plans are followed through the course of the studies
Sets and manages Data Management project timelines
Provides comprehensive status updates to project team members
Address data issues identified by cross-functional team members, accountable for external data vendor documentation, management, and reconciliation
Assist in defining and creating data listings, summary table validation, data specifications, and process data transfers in preparation for statistical review and data management audit
Implements data standardization and maintains 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.
501-1000 employees
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
Leadership Team
Luan Wilfong
Chief Human Resources Officer
Steve Kelsey
President
Recent News
Pharmaceutical Technology
2026-01-13
Company data provided by crunchbase