Revolution Medicines
Executive Medical Director, GI, Europe(m/w/x)
Full-timeOn-siteSenior
Basel
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RORoche
Global Medical Affairs Lead Genomic Profiling(m/w/x)
Basel
Full-timeOn-siteSenior
Nejo AI Summary
Global medical strategy for genomic profiling evidence generation and investigator-initiated studies. Advanced degree and 5+ years oncology/hematology medical affairs experience required. Educational content development and clinical data delivery.
Requirements
- Extensive knowledge in cancer genomics
- Advanced degree (MD and/or PhD) in related disciplines
- 5+ years industry experience in oncology/hematology medical affairs/development
- Leading design/implementation of clinical studies
- Leading scientific communication and educational efforts
- Deep understanding of molecular-guided therapeutic approaches
- Deep understanding of clinical practice guidelines
- Translating genomics/real-world data into clinically relevant actions
- Excellent English oral and written communication skills
- Ability to develop medical content
- Confident presentation to diverse audiences
- Proactive and self-directed
- Proven track record of leading global programs
- Strategic decision making
- Systems thinking
- Adaptability in complex environments
- Deep understanding of legal considerations in healthcare industry
- Deep understanding of regulatory considerations in healthcare industry
- Deep understanding of biopharma and diagnostics industry considerations
- Willingness to travel up to 20%
Tasks
- Provide strategic medical and scientific input
- Lead global medical strategies for evidence generation
- Conduct investigator-initiated studies and research collaborations
- Execute medical activities like advisory boards and scientific symposia
- Develop and deliver educational content and clinical data
- Build partnerships with medical and patient communities
- Drive safe adoption of genomic profiling solutions
- Ensure operational excellence and compliance with regulations
- Communicate science and clinical data effectively
- Partner across functions, regions, and cultures
- Champion patient and customer-centricity
- Model Roche’s values of integrity, courage, and passion
- Adhere to legal, regulatory, and company standards
- Handle compliance questions and considerations
- Complete required training and documentation
- Coach colleagues with less experience
- Work independently and autonomously
Work Experience
- 5 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 Roche 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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RORoche
Global Medical Affairs Lead Genomic Profiling(m/w/x)
Basel
Full-timeOn-siteSenior
Nejo AI Summary
Global medical strategy for genomic profiling evidence generation and investigator-initiated studies. Advanced degree and 5+ years oncology/hematology medical affairs experience required. Educational content development and clinical data delivery.
Requirements
- Extensive knowledge in cancer genomics
- Advanced degree (MD and/or PhD) in related disciplines
- 5+ years industry experience in oncology/hematology medical affairs/development
- Leading design/implementation of clinical studies
- Leading scientific communication and educational efforts
- Deep understanding of molecular-guided therapeutic approaches
- Deep understanding of clinical practice guidelines
- Translating genomics/real-world data into clinically relevant actions
- Excellent English oral and written communication skills
- Ability to develop medical content
- Confident presentation to diverse audiences
- Proactive and self-directed
- Proven track record of leading global programs
- Strategic decision making
- Systems thinking
- Adaptability in complex environments
- Deep understanding of legal considerations in healthcare industry
- Deep understanding of regulatory considerations in healthcare industry
- Deep understanding of biopharma and diagnostics industry considerations
- Willingness to travel up to 20%
Tasks
- Provide strategic medical and scientific input
- Lead global medical strategies for evidence generation
- Conduct investigator-initiated studies and research collaborations
- Execute medical activities like advisory boards and scientific symposia
- Develop and deliver educational content and clinical data
- Build partnerships with medical and patient communities
- Drive safe adoption of genomic profiling solutions
- Ensure operational excellence and compliance with regulations
- Communicate science and clinical data effectively
- Partner across functions, regions, and cultures
- Champion patient and customer-centricity
- Model Roche’s values of integrity, courage, and passion
- Adhere to legal, regulatory, and company standards
- Handle compliance questions and considerations
- Complete required training and documentation
- Coach colleagues with less experience
- Work independently and autonomously
Work Experience
- 5 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 Roche 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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Roche
Industry
Pharmaceuticals
Description
The company is dedicated to advancing science and ensuring access to healthcare for everyone.
Not a perfect match?
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