Intern, Clinical Operations Execution Optimization

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS‑addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors daraxonrasib (RMC‑6236), a RAS(ON) multi‑selective inhibitor; elironrasib (RMC‑6291), a RAS(ON) G12C‑selective inhibitor; zoldonrasib (RMC‑9805), a RAS(ON) G12D‑selective inhibitor; and RMC‑5127, a RAS(ON) G12V‑selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity

The Clinical Operations Summer Intern will support a strategic initiative focused on optimizing study‑level execution and operational alignment to the Clinical Operations Handbook (V2.0). The intern will conduct a structured review of active clinical studies to assess consistency, tool utilization, and workflow execution from protocol finalization through site activation.

Key Responsibilities

• Select 1–2 active clinical studies for detailed assessment.
• Evaluate use of RAID logs, Study Dashboards, Vendor Oversight Plans, and Startup Timelines.
• Document end‑to‑end workflows from protocol finalization to site activation.
• Identify gaps, redundancies, and inconsistencies in process execution.
• Conduct structured interviews with COLs and CTAs.
• Shadow CSET meetings to observe dashboard and RAID utilization.
• Review Smartsheet tools and Egnyte folder structures.
• Compare real‑world execution against Clinical Operations Handbook processes.

Deliverables

• Current‑state workflow maps with annotated pain points.
• Tool consistency matrix across selected studies.
• Prioritized, actionable process improvement recommendations.
• Updated mock dashboard or tracker templates (if applicable).

Impact

• Reduce variability in study‑level execution.
• Clarify ownership and functional handoffs.
• Improve dashboard clarity for leadership review.
• Strengthen inspection readiness through documented alignment.

Required Skills, Experience and Education

• Pursuing a Bachelor’s or Master’s degree in Life Sciences, Public Health, Clinical Research, Business, or related field.
• Excellent communication skills.
• Interest in clinical trial operations and process optimization.

Preferred Skills

• Strong analytical and organizational skills.
• Proficiency in Microsoft Office; familiarity with Smartsheet a plus.

Base Pay Salary Range

$67,000 - $81,000 USD

EEO Statement

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.