Medical Affairs Manager (m/f/d)
Munich, Bavaria, Germany · Full Time
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- Experience
- 3+ yrs
- Salary
- —
- Openings
- 1
- Posted
- 3 weeks ago
- Work mode
- In office
- Education
- MD/PharmD/PhD
- Eligibility
- Professionals with a scientific or medical doctorate-level background and relevant pharmaceutical industry experience, especially those with medical affairs exposure and the ability to work in German and English, are suitable for this role.
- Resume
- Required to apply
Where you'll work
Job description
Role Overview
ProPharma positions medical affairs as a core part of how science is translated into strategy and better outcomes for patients. In this role, you will work with pharmaceutical and biotechnology clients on complex scientific and medical challenges, helping advance innovation and support therapies through different stages of their lifecycle.
This opportunity is suited to a medical affairs professional who is comfortable moving between scientific discussion, project leadership, and stakeholder collaboration. The role calls for someone who can assess clinical data, shape medical direction, question assumptions, and build reliable working relationships.
Key Contributions
- Convert clinical data into clear, accurate, and persuasive scientific messaging.
- Support launch preparation and help products progress effectively into new lifecycle phases.
- Apply medical expertise to clinical research and broader evidence-generation work.
- Check scientific documents for accuracy, scientific balance, and compliance with regulations.
- Share data and insights with different audiences, including healthcare professionals and internal cross-functional teams.
- Work through uncertainty, keep priorities organised, and advance workstreams in fast-changing settings.
- Develop dependable partnerships with colleagues, clients, and external stakeholders.
Profile Sought
- Medical degree, PharmD, or PhD in life sciences or a closely related field.
- Several years of experience in the pharmaceutical industry, with oncology experience preferred.
- Background in medical affairs or a comparable scientific function.
- Practical exposure to product launches and lifecycle management.
- Understanding of clinical development and evidence-generation activities.
- Ability to review scientific materials in regulated environments with confidence.
- Strong communication skills with the ability to simplify complex science for different audiences.
- Well-organised working style with the flexibility to adapt when priorities shift.
- Fluent written and spoken German and English.
- Readiness to travel according to project and client requirements.
Additional Information
This position is based in Munich, Bavaria, Germany and is offered as a full-time onsite role. No salary, stipend, vacancy count, or start date has been specified.