Intern, Clinical Trial Operations, Clinical Operations

Revolution Medicines • Redwood City, CA

19h • $67,000 - $81,000 • Hybrid

About The Position

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: This is a unique opportunity as a junior Clinical Trial Assistant in Clinical Operations, initially reporting to the Associate Director/Director Clinical Operations, you will be responsible for acting as a central contact for the clinical study teams and assist with the clinical execution and management to support RevMed clinical trials.

Requirements

• Currently enrolled at an accredited college/university as a rising senior or higher in a Bachelor’s degree in biological sciences or related health related field.
• 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 and interpersonal skills.
• Demonstrate proficiency in Microsoft Word, Excel and PowerPoint and other software platforms.
• Demonstrated ability to multi-task, prioritize options.

Responsibilities

• Assisting in the review, distributing, and archiving of study specific documents and reports (plans, training materials, study guides, manuals etc.).
• Assisting with updating and maintaining clinical systems and any reporting tools.
• Support maintenance of the trial master files (TMF) if applicable, or work with CRO to audit and resolve discrepancies.
• Create, maintain, and track information for key study related activities.
• Assisting in the preparation of meeting materials, scheduling meetings, for internal clinical operation team meetings.
• Working with cross functional study teams, and vendors to assist in the coordination of clinical trial activities.
• Support other clinical operations activities as appropriate.

What This Job Offers

• Career Level: Intern
• Number of Employees: 251-500 employees