Senior Manager, Medical Science Liaison
New
R
Revolution MedicinesBiotech Oncology
Remote (Japan)Full-TimeManager
Salary not disclosed
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Job Details
- Languages
- Japanese and English (business level)
- Experience
- Minimum 5 years of experience in Medical Affairs or related functions in the pharmaceutical or biotech industry.
Requirements
- Minimum 5 years of experience in Medical Affairs or related functions in the pharmaceutical or biotech industry.
- Strong understanding of oncology clinical development, evidence generation, and treatment landscape.
- Proven ability to analyze and synthesize scientific information effectively.
- Experience engaging with healthcare professionals, academic researchers, and medical societies with compliance rules.
- Excellent interpersonal, organizational, and presentation skills.
- Fluency in Japanese and English (business level).
- Ability to work effectively in a matrixed, cross-functional, and multicultural environment.
- Willingness to travel up to 70% of time.
Responsibilities
- Support the implementation and execution of the Medical Affairs strategy and tactical plans for assigned products and therapeutic areas, tailored to Japan.
- Establish and maintain trusted scientific relationships with key opinion leaders (KOLs), investigators, and healthcare professionals across Japan.
- Provide medical oversight and scientific input to cross-functional teams, ensuring alignment with regulatory and compliance standards.
- Contribute to medical input in promotional and non-promotional materials, internal training, and advisory boards.
- Plan and execute medical meetings, education, symposia, and congress participation to enhance scientific visibility.
- Support investigator-initiated trials and local clinical research activities in collaboration with global and regional teams.
- Monitor the competitive and scientific landscape to inform internal strategy and provide actionable medical insights.
- Partner with HEOR and market access to develop real-world evidence and outcomes research projects.
- Collaborate closely with Clinical Operations and CROs, including site selection, Site Initiation Visits, and investigator engagement.
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