Medical Affairs Manager, (m/f/d)

At ProPharma, medical affairs is more than a support function. It is where science, strategy, and patient impact come together. We partner with pharmaceutical and biotechnology companies to solve complex challenges, support innovation, and help bring meaningful therapies to patient s.

We are looking for a Medical Affairs professional who enjoys working where scientific expertise meets real-world decision-making. Someone who is equally comfortable discussing clinical evidence, leading projects, challenging assumptions, and building trusted relationships.

What you will contribute

You will act as a scientific partner across projects, helping translate complex evidence into meaningful insights and practical actions. Depending on the assignment, you may support product launches, guide medical strategies, contribute to clinical programs, or advise stakeholders on scientific and medical topics. Your work may include:

• Turning clinical evidence into clear and credible scientific communication
• Supporting launch readiness and helping products successfully enter new stages of their lifecycle.
• Contributing medical expertise to clinical studies and evidence-generation activities.
• Reviewing scientific content to ensure accuracy, balance, and compliance.
• Presenting data and insights to diverse audiences, from healthcare professionals to cross-functional teams.
• Navigating ambiguity, managing priorities, and moving projects forward in changing environments.
• Building trusted partnerships internally and externally

Who you are

You combine scientific depth with practical thinking. You ask questions, challenge assumptions, and enjoy finding solutions where others see complexity. You'll bring:

• An MD, PharmD, or PhD in Life Sciences or a related discipline.
• Several years of experience within the pharmaceutical industry, ideally including oncology.
• Experience in medical affairs or similar scientific roles.
• Exposure to product launches and lifecycle management activities.
• Understanding of clinical development and medical evidence generation.
• Confidence reviewing scientific materials within regulated environments.
• Strong communication skills and the ability to make complex science accessible.
• An organized and structured approach while remaining flexible when priorities change.
• Fluency in German and English, both written and spoken.
• A willingness to travel as projects and client needs require.