Senior Manager, Global Medical Information

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys 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 Revolutionariesin a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

As a key member of the Global Medical Affairs team the Senior Manager Global Medical Information will be supporting the development enhancement and day-to-day operations of the medical information function to advance RevMeds pipeline and future commercial growth. This individual will help implement medical information strategies content plans systems and processes to ensure timely accurate and scientifically balanced responses to healthcare professionals and internal stakeholders.

The Senior Manager will partner closely with medical Information leadership and collaborate with Medical Affairs Clinical Development Regulatory Legal/Compliance Commercial and external vendors to support global medical information capabilities including medical inquiry management medical content development knowledge management and communications processes.

Key responsibilities include:

Global Medical Information Strategy and Operations

• Support development and operations of the Medical Information function in partnership with Medical Information leadership to support the oncology pipeline and launch readiness.

• Manage and continuously improve processes for medical inquiry intake triage response documentation reporting and analytics.

• Support development maintenance and optimization of digital Medical Information assets including Medical Affairs website.

• Collaborate with regional medical teams to ensure consistent delivery of medical information worldwide.

• Provide project-level support for medical information and cross-functional initiatives as needed.

Content Development & Review

• Partner with cross-functional stakeholders to support timely development and approval of medical information resources.

• Manage creation review and maintenance of global medical response content and scientific FAQs to ensure accuracy alignment with data labeling and medical strategy and compliance with relevant guidelines (e.g. PHRMA Code FDA regulations).

Inquiry Management & Vendor Oversight

• Support oversight of vendor partners responsible for medical information inquiry handling and systems operations ensuring quality compliance and timely execution.

• Monitor inquiry volume trends and response quality to identify insights inform training needs and recommend process improvements.

• Contribute to global consistency in medical information delivery and support development of scalable processes to meet future commercial needs.

Congress support

• Provide medical information support at medical congress booths including coordination of booth materials and supporting internal booth training.

• Serve as a scientific resource during congresses to address medical inquiries and support compliant insight collection and documentation.

Cross-Functional Collaboration & Compliance

• Support call center readiness training and development of SOPs and operational tools for future product launches.

• Ensure timely escalation and communication of safety-related information in collaboration with Pharmacovigilance.

• Support inspection and audit readiness by maintaining accurate documentation and supporting process control activities.

Required Skills Experience and Education:

• Bachelors degree required in a life science or health-related field.

• Bachelors degree required; advanced scientific degree (PharmD PhD MD MS) strongly preferred.

• Minimum of 9 years of relevant experience with a Bachelors degree 7 years with a Masters degree or 5 years with a PharmD PhD or MD; experience in Medical Information within the pharmaceutical or biotech industry preferred.

• Experience in oncology strongly preferred.

• Demonstrated experience developing global medical response materials and medical information processes.

• Understanding of medical information regulations and industry standards (e.g. FDA GPP PhRMA ICMJE).

• Experience managing medical inquiry databases and medical information vendors.

• Proven ability to collaborate effectively across functions and build scalable systems and processes.

• Ability to liaise with cross-functional teams including Medical Affairs Legal Compliance Finance and IT.

Preferred Skills:

• Experience supporting product launches and establishing medical information functions in a growing organization.

• Familiarity with Veeva CRM and medical inquiry systems/databases.

• Experience in oncology or precision medicine is a plus.

• Prior experience working in a fast-paced matrixed biotech or pharmaceutical environment.

• Familiarity with emerging digital tools for Medical Information operations and engagement. #LI-Hybrid #LI-YG1