Revolution Medicines
Executive Medical Director, GI, Europe(m/w/x)
Full-timeWith HomeofficeSenior
Basel
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RERevolution Medicines
Senior Medical Director, Midsize Markets Europe(m/w/x)
Basel
Full-timeRemoteSenior
Nejo AI Summary
Medical strategy and execution for novel targeted therapies in precision oncology for RAS-addicted cancers. Advanced degree (MD/PhD) and 10+ years' Medical Affairs experience with country leadership track record required. Direct impact on novel targeted therapy development.
Requirements
- Advanced degree (MD or PhD)
- Strong background/experience in oncology
- 10+ years' experience in Medical Affairs with country leadership track record
- Experience with scientific data generation, clinical trial interpretation, and complex data communication
- Proven value/benefit assessment experience
- Deep understanding of midsized markets access, local healthcare systems, and regulatory landscape
- Strong stakeholder management
- Ability to collaborate with internal/external partners
- Proven experience supporting oncology product launches in European market
- Experience in biotech
- Excellent communication skills (in-person and virtual)
- Proven leadership and people management capabilities
- Success in fast-growing, entrepreneurial environment
- Strong leadership presence
- Adaptability and flexibility
- Scientific and solution-oriented mindset
- Capability to execute in rapidly changing, ambiguous environment
- Strong understanding of local healthcare systems, customer dynamics, and reimbursement environment
- Highly organized and motivated
- Excellent communication, presentation, and interpersonal skills
- Ability to thrive in fast-paced, dynamic environment
- Ability to adjust priorities and workload
- Willingness to travel nationally and internationally
Tasks
- Lead medical strategy and execution for MidSized Markets
- Drive medical impact across the RevMed portfolio
- Serve on the Midsized Markets Leadership Team
- Contribute insights to medical and clinical development strategy
- Inform launch planning and business decisions
- Establish medical strategy for pre-launch, launch, and post-launch phases
- Align efforts with access, regulatory, and commercial objectives
- Build and execute the medical plan
- Collaborate with regional and global teams on medical strategy
- Partner with local, regional, and global clinical development teams
- Partner with local, regional, and global operations teams
- Translate global medical and clinical strategies
- Represent the company as a senior medical expert
- Engage with local oncology and scientific communities
- Act as a spokesperson for Midsized markets
- Gather, analyze, and interpret clinical data
- Provide strategic insights for critical decisions
- Build relationships with national key opinion leaders
- Build relationships with oncology networks, academic institutions, and scientific societies
- Lead scientific exchange and advisory boards
- Lead investigator and external meetings
- Lead press conferences and country-level congress engagement
- Provide medical leadership for evidence generation activities
- Oversee local studies and real-world evidence initiatives
- Oversee investigator-initiated research (where permitted)
- Ensure execution of publication plans
- Ensure execution of scientific communication activities
- Lead medical launch readiness for oncology products
- Develop launch training and scientific materials
- Develop field medical engagement plans
- Partner with Market Access and Commercial teams
- Support value communication and reimbursement interactions
- Represent evidence at HTA hearings
- Define innovation value at HTA hearings
- Support lifecycle management activities
- Support new indications and label updates
- Support competitive positioning
- Review and approve non-promotional materials
- Ensure compliance with local regulations
- Ensure compliance with national and EFPIA codes
- Ensure compliance with internal company policies
- Recruit country Medical teams, including Medical Directors and MSLs
- Establish medical processes, governance, and ways of working
- Foster a culture of scientific rigor, compliance, and collaboration
- Represent Medical Affairs in governance forums
- Represent Medical Affairs in risk management forums
Work Experience
- 10 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Revolution Medicines and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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RERevolution Medicines
Senior Medical Director, Midsize Markets Europe(m/w/x)
Basel
Full-timeRemoteSenior
Nejo AI Summary
Medical strategy and execution for novel targeted therapies in precision oncology for RAS-addicted cancers. Advanced degree (MD/PhD) and 10+ years' Medical Affairs experience with country leadership track record required. Direct impact on novel targeted therapy development.
Requirements
- Advanced degree (MD or PhD)
- Strong background/experience in oncology
- 10+ years' experience in Medical Affairs with country leadership track record
- Experience with scientific data generation, clinical trial interpretation, and complex data communication
- Proven value/benefit assessment experience
- Deep understanding of midsized markets access, local healthcare systems, and regulatory landscape
- Strong stakeholder management
- Ability to collaborate with internal/external partners
- Proven experience supporting oncology product launches in European market
- Experience in biotech
- Excellent communication skills (in-person and virtual)
- Proven leadership and people management capabilities
- Success in fast-growing, entrepreneurial environment
- Strong leadership presence
- Adaptability and flexibility
- Scientific and solution-oriented mindset
- Capability to execute in rapidly changing, ambiguous environment
- Strong understanding of local healthcare systems, customer dynamics, and reimbursement environment
- Highly organized and motivated
- Excellent communication, presentation, and interpersonal skills
- Ability to thrive in fast-paced, dynamic environment
- Ability to adjust priorities and workload
- Willingness to travel nationally and internationally
Tasks
- Lead medical strategy and execution for MidSized Markets
- Drive medical impact across the RevMed portfolio
- Serve on the Midsized Markets Leadership Team
- Contribute insights to medical and clinical development strategy
- Inform launch planning and business decisions
- Establish medical strategy for pre-launch, launch, and post-launch phases
- Align efforts with access, regulatory, and commercial objectives
- Build and execute the medical plan
- Collaborate with regional and global teams on medical strategy
- Partner with local, regional, and global clinical development teams
- Partner with local, regional, and global operations teams
- Translate global medical and clinical strategies
- Represent the company as a senior medical expert
- Engage with local oncology and scientific communities
- Act as a spokesperson for Midsized markets
- Gather, analyze, and interpret clinical data
- Provide strategic insights for critical decisions
- Build relationships with national key opinion leaders
- Build relationships with oncology networks, academic institutions, and scientific societies
- Lead scientific exchange and advisory boards
- Lead investigator and external meetings
- Lead press conferences and country-level congress engagement
- Provide medical leadership for evidence generation activities
- Oversee local studies and real-world evidence initiatives
- Oversee investigator-initiated research (where permitted)
- Ensure execution of publication plans
- Ensure execution of scientific communication activities
- Lead medical launch readiness for oncology products
- Develop launch training and scientific materials
- Develop field medical engagement plans
- Partner with Market Access and Commercial teams
- Support value communication and reimbursement interactions
- Represent evidence at HTA hearings
- Define innovation value at HTA hearings
- Support lifecycle management activities
- Support new indications and label updates
- Support competitive positioning
- Review and approve non-promotional materials
- Ensure compliance with local regulations
- Ensure compliance with national and EFPIA codes
- Ensure compliance with internal company policies
- Recruit country Medical teams, including Medical Directors and MSLs
- Establish medical processes, governance, and ways of working
- Foster a culture of scientific rigor, compliance, and collaboration
- Represent Medical Affairs in governance forums
- Represent Medical Affairs in risk management forums
Work Experience
- 10 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Revolution Medicines and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Revolution Medicines
Industry
Pharmaceuticals
Description
The company is a clinical-stage precision oncology company focused on developing novel targeted therapies for RAS-addicted cancers.
Not a perfect match?
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