Senior Medical Director, Midsize Markets Europe

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 Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

Reporting to the VP GM Midsized Markets the Senior Medical Director Midsize Markets Europe is the medical leader responsible for defining and executing the medical strategy for oncology products in our portfolio within Midsized markets. This role serves as the medical voice within the Midsized markets Leadership Team ensuring scientific excellence compliant medical engagement and strong alignment between global strategy and local patient physician and healthcare system needs. This leader will ensure that Midsized markets medical considerations are embedded in the regional medical strategy and plans and will partner with the Midsized markets country managers and crossfunctional teams as well as VP Head of Europe Medical Affairs and their leadership team. The incumbent will contribute to building the Midsized markets medical team and working closely with the Global Regional Country Medical Affairs teams across Med Affairs functions.

Responsibilities:

• Act as the Medical lead for MidSized Markets accountable for medical strategy execution and impact across the RevMed portfolio.

• Serve as a core member of the Midsized Markets Leadership Team contributing insights to medical and clinical development strategy launch planning and business decisions.

• Establish Midsized markets medical strategy across pre-launch launch and post-launch phases.

• Oversee all aspects of medical strategy and execution in Midsized markets.

• Cross-functionally align efforts seamlessly with access regulatory and commercial objectives while building and executing upon the medical plan.

• Collaborate effectively with regional and global teams by contributing to overall medical strategy strongly partnering with local regional and global clinical development and operations teams.

• Translate global medical and clinical strategies into relevant medical strategy.

• Represent the company as the senior medical expert within the local oncology and scientific community acting as a spokesperson for Midsized markets.

• Gather analyze and interpret clinical data providing strategic insights to inform critical decisions.

• Build strong relationships with national key opinion leaders oncology networks academic institutions and scientific societies.

• Lead scientific exchange advisory boards investigator and other external meetings press conferences and congress engagement at country level.

• Provide medical leadership on evidence generation activities including local studies real-world evidence initiatives and investigator-initiated research (where permitted).

• Ensure effective execution of publication plans and scientific communication activities.

• Lead medical launch readiness for oncology products including training scientific materials and field medical engagement plans.

• Partner with Market Access and Commercial country and regional teams to support value communication and reimbursement-related interactions from a medical perspective e.g. representing and defining evidence and value of innovation at oral HTA hearings.

• Support lifecycle management activities including new indications label updates and competitive positioning.

• Provide medical review and approval of non-promotional materials in accordance with local regulations and company policies.

• Help recruit country Medical teams including Medical Directors and Medical Science Liaisons.

• Establish medical processes governance and ways of working as part of the Midsized markets build-out.

• Foster a culture of scientific rigor compliance and collaboration.

• Ensure all medical activities comply with local regulations national and EFPIA codes and internal company policies.

• Represent Midsized markets Medical Affairs in company governance and risk management forums.

Required Skills Experience and Education:

• Advanced degree required (MD or PhD).

• Strong background and experience in oncology required.

• 10 years experience in Medical Affairs with a track record of country leadership.

• Experience with scientific data generation clinical trial interpretation and communication of complex data to diverse audiences.

• Proven value and benefit assessment experience with deep understanding of midsized markets access local healthcare systems and regulatory landscape.

• Strong stakeholder management and ability to collaborate with internal and external partners.

• Proven experience supporting oncology product launches in a European market.

• Experience in biotech.

• Excellent communication skills both in person and virtual.

• Proven leadership and people management capabilities; demonstrated success in small but fast growing entrepreneurial environment.

• Demonstrated strong leadership presence.

• Has demonstrated adaptability and flexibility.

• Scientific and solution-orientated mindset and capability to move and execute in a rapidly changing ambiguous environment.

• Strong understanding of local healthcare systems customer dynamics and reimbursement environment.

• Highly organized and motivated individual possessing excellent communication presentation and interpersonal skills. Thrives in a fast-paced dynamic small company environment and able to adjust priorities and workload based upon changing needs.

• Willingness to travel nationally and internationally.

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