Associate Director, Data Standards and EDC Programming
Revolution Medicines · Redwood City, California, United States · $186k–$233k
Posted by Revolution Medicines on their careers site · View the original posting
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The posting, as Revolution Medicines wrote it
Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.
Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.
The Opportunity
The Associate Director of Data Standards and EDC Programming is responsible for clinical data collection standards and Medidata Rave programming at Revolution Medicines. The role manages the continued development of the Rave Global Library and oversees study builds, core system configurations, and programming work performed by external partners.
Reporting to the Senior Director, Clinical Data Systems & Ops Ex, the Associate Director works with Clinical Data Management, IT, Statistical Programming, Clinical Operations, and other study team members to plan and deliver EDC work. Responsibilities include maintaining standards, resolving technical issues, managing vendor performance, and overseeing testing and controlled system changes.
This position requires practical experience building studies in Medidata Rave and the judgment to decide when a standard should be used, revised, or adapted for a study. The Associate Director is expected to reduce repeated programming work, improve build quality, and help study teams meet their timelines.
Responsibilities
Manage EDC programming staff and external programming partners. Assign work, review deliverables, provide technical guidance, and support staff development.
Set priorities and resource plans for EDC programming and data standards work. Agree on timelines with study teams, manage competing requests, and bring delivery risks and resource needs to management.
Maintain and expand the Medidata Rave Global Library, including core and oncology eCRFs, edit checks, derivations, custom functions, dictionaries, and study templates.
Oversee Rave study builds, protocol amendments, database migrations, and production changes. Work with Data Management to confirm requirements and assess the effect of changes on existing data and study processes.
Review build specifications and programming deliverables and provide hands-on support for complex Rave configurations and C# custom functions.
Manage core Rave configurations and coordinate user access, site administration, security settings, and study archival activities with IT, Data Management, and vendors.
Serve as the primary EDC prog
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anges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
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Base Pay Salary Range
$186,000 — $233,000 USD
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