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: Assist with the oversight of the Pharmacovigilance Contract Research Organization (PV CRO) performing case management and study support activities. Assist with the management of the PV CRO to ensure compliance within the required timelines. Provide vendors with relevant clinical study documents and updates. Coordinate the review and filing of study plans and associated documents. Coordinate the review and filing of PV CRO documents and monthly compliance reports. Track and maintain well-organized department files, including listings and trackers received from CROs. Support eTMF oversight of safety case files and relevant documents with PV and clinical CROs. Participate and review TMF plans to capture PV and clinical CRO’s filing responsibilities. Maintain PV CRO distribution contact lists and oversee Clinical CRO site contact lists. Maintain meeting materials, schedule meetings, develop agendas, and track meeting minutes. Assist with MedDRA and WHO Drug coding impact analysis review. Prepare aggregate periodic reports for departmental review and CRO distribution. Assist with Standard Operating Procedure (SOP) cross-functional review in Quality Management System. Perform administrative tasks to support GPS team, as needed. Support GPS Operations team in other PV activities as appropriate to experience and expertise.