Clinical Trial Assistant

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.  The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

This is a unique opportunity for an entry-level Clinical Operations Professional. As a Clinical Trial Assistant (CTA), you will be responsible for providing administrative and operational support for one or more studies within a clinical program. Reporting into the Sr. Clinical Program Manager, you will play a critical role in executing well-defined tasks that support clinical study start-up, maintenance, and close-out.

Responsibilities:

• Work on assignments and problems of limited scope, requiring independent decision-making and initiative, using standard procedures under close supervision.

• Solicit Clinical Study Execution Team (CSET) meeting agenda topics, coordinate meetings, minutes, and logistical support.

• Support site management activites and provide status to CSET (e.g., tracking site documents, distributing study materials, site enrollment metrics, etc.).

• Liaise with internal teams and vendors for document collection and update; act as primary CTA contact on studies.

• File study documents to the Trial Master File (TMF) and assist with TMF reviews. Maintain TMF and ensure document quality and completeness.

• May assist with protocol amendment documentation and version control.

• May assist with development of basic department initiatives, process documents, and standard forms most used by CTAs.

• Support other clinical operations activities as appropriate.

Required Skills, Experience and Education:

• BS, BA, or RN in a relevant scientific discipline.

• 0-3 years of relevant experience in the pharmaceutical or biotech industry, preferably in Clinical Operations or Clinical Research related experience.

• Basic understanding of FDA and EMA Regulations, ICH guidelines, GCP, and familiarity with standard clinical operation procedures (SOPs).

• Basic organization and communication skills.

• Proficient in MS Office (Word, Excel, Outlook) and project tracking tools.

• Demonstrate reliability, proactive communication, and quality in task execution.

• Apply knowledge of Clinical Operations in day-to-day assigned tasks.

• Thrive in a collaborative team setting and be driven by a desire to deploy innovative approaches and technologies in a high-energy environment.

• Travel may be required (~10%).

Preferred Skills:

• Has familiarity working with vendor systems/portals (e.g., eTMF, EDC, IRT, CTMS).

• Oncology experience preferred. #LI-Hybrid #LI-JC1