Revolution Medicines→
Intern, Clinical Supply Chain at Revolution… · San…
InternshipOn-siteSan Francisco Bay Area$67k–$81k/yr
Skills
clinical trial operationsprocess optimizationmicrosoft officesmartsheetproject management toolsclinical researchregulated environmentsanalytical skills
Job Description
Summary: Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. They are seeking a motivated Summer Intern to support a strategic Clinical Operations initiative focused on optimizing study-level execution and alignment with internal Clinical Operation tools. The intern will gain hands-on exposure to cross-functional clinical trial operations while delivering actionable process improvement insights.
Responsibilities:
- Review one to two active clinical studies for detailed operational assessment
- Evaluate utilization of key study management tools including logs used for study tracking, e.g., risks, actions, issues, decisions
- Study Dashboards, Vendor Oversight Plans, and Study Startup Timelines
- Document end-to-end workflows from protocol finalization through site activation
- Identify gaps, redundancies, and inconsistencies in process execution across studies
- Conduct structured interviews with Clinical Operations Leads (COLs) and Clinical Trial Assistants (CTAs)
- Shadow Clinical Study Execution Team (CSET) meetings to observe dashboard and RAID log utilization
- Review Smartsheet tools and Egnyte folder structures to assess organization and consistency
- Compare real-world study execution against documented Clinical Operations Handbook processes
Required Qualifications:
- Currently pursuing a Bachelor's or Master's degree in Life Sciences, Public Health, Clinical Research, Business, or related field
- Strong analytical and organizational skills
- Effective written and verbal communication skills
- Proficiency in Microsoft Office (Word, Excel, PowerPoint)
- Interest in clinical trial operations and process optimization
Preferred Qualifications:
- Familiarity with Smartsheet or similar project management tools
- Prior exposure to clinical research or regulated environments
Required Skills: Clinical trial operations, Process optimization, Microsoft Office, Smartsheet, Project management tools, Clinical research, Regulated environments, Analytical skills
Benefits: Competitive cash compensation, Robust equity awards, Strong benefits, Significant learning and development opportunities
Benefits
Competitive cash compensation
Robust equity awards
Strong benefits
Significant learning and development opportunities