Revolution Medicines
Clinical Trial Assistant
Revolution Medicines, Redwood City, California, United States, 94061
Overview
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.
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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
#J-18808-Ljbffr