Executive Medical Director, GI, 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 Medical Affairs Europe the Executive Medical Director GI Europe provides strategic medical leadership across the European region for the GI oncology portfolio. This role will be responsible for defining and executing the Regional medical strategy in alignment with global objectives ensuring scientific excellence patient- centricity and compliance. The position serves as a key medical partner to global team regional leadership and external stakeholders and acts as a medical expert in GI Oncology. A key focus of the position is to prepare and support the upcoming launches working in close collaboration with the full cross functional team including Commercial Market Access Regulatory Clinical Development and Global Medical Affairs. As such the role requires a highly collaborative leader who can effectively operate in a matrix environment influence without authority and foster strong partnerships to ensure successful and compliant launches. The role will be based in Switzerland.

Responsibilities:

• Lead the development and execution of the Regional GI medical strategy and medical objectives including activities related to scientific engagement and communication evidence generation internal education and patient advocacy.

• Act as a strategic partner to Global Medical Affairs R&D Market Access Commercial and Regulatory teams.

• Translate global medical strategy into impactful regional plans aligned with European market needs and scientific priorities.

• Oversee European Medical input into clinical development real-world evidence and publication strategy by leading the development and execution of a Healthcare Professional engagement strategy to gather insights to shape internal programs.

• Serve as the senior medical authority for GI oncology in Europe ensuring high scientific and ethical standards.

• Participate in the Regional Medical Affairs Team to execute medical strategies contribute to the operations and oversight of medical activities and work cross-functionally to support associated pre-launch activities in GI.

• Contribute to the execution of routine gap assessments leading to the development/refinement of launch strategy an evidence generation plan and tactical plan as part of the overall regional medical plan.

• Guide scientific exchange activities including advisory boards congress strategy investigators interaction and medical education.

• Communicate clinical and scientific data to Key external experts and other healthcare professionals through presentations educational programs and scientific discussions.

• Represent various medical affairs functions in cross-functional strategy team meetings including Clinical and Safety sub-teams Regional and Global Brand Team Regional and Global GI Team Patient Advocacy Market Access and other cross-functional strategic discussions.

• Partner with the Clinical and MSL teams to provide enrollment scientific and engagement support to ensure clinical trials meet study timelines.

• Partner with RWE/HEOR strategy and activities as part of the Regional medical Plan.

• Partner with the Patient Advocacy and Grants teams to incorporate the patient voice and define external medical education strategies for independent grants respectively.

• Provide medical expertise for scientific symposia and medical congresses and collaborate across relevant functions to develop review and align on key scientific communication points and medical information response documents within legal and compliance guidelines.

• Ensure compliance with all applicable regulatory pharmacovigilance and medical governance requirements.

Required Skills Experience and Education:

• An advanced degree (MD PhD) in medical/scientific area is required.

• 15 years of relevant experience in the biotech or pharmaceutical industry focused on Medical Affairs with regional cross-functional in-house experience and on field-based teams.

• Must have a strong scientific background in oncology with a good understanding of biomarker-driven disease and ability to effectively analyze synthesize and communicate complex scientific information.

• Direct hands-on experience executing the activities of various functions within medical affairs (training medical communications medical information expanded access programs evidence generation publications).

• Proven track record of clinical trial support including protocol development/review site selection support enrollment support and data analysis.

• Excellent interpersonal written and presentation skills with the ability to effectively communicate complex scientific data with a strong point of view to diverse audiences.

• Thrives in fast-paced dynamic environment and ability to multi-task independently with limited supervision.

• Ability to travel in Europe and international congresses.

• Strong networking skills with deep existing relationships with oncology healthcare professionals including regional top key opinion leaders required.

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

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

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