Associate Medical Director

Position Title : Medical Lead Oncology – Germany

Location : 100% Home Office

Reports to : Medical Director Germany

Position Summary

This is an exceptional opportunity to join a dynamic and agile oncology-focused organization at a pivotal time of growth. With two oncology products recently authorized in Europe and a robust pipeline ahead, the company is expanding its footprint and impact across the region.

As Medical Lead Oncology – Germany , you will play a strategic and hands-on leadership role in shaping and executing the medical affairs strategy for the solid tumors portfolio. You will lead a dedicated team, drive scientific excellence, and collaborate cross-functionally to ensure successful product launches and lifecycle management. This role offers the chance to make a meaningful difference for patients while working in a highly collaborative and entrepreneurial environment.

Key Responsibilities

• Lead, develop, and manage the solid tumors medical team in Germany, including five direct reports (Medical Advisor and four MSLs).
• Drive the development and tactical execution of local medical launch and lifecycle management activities in alignment with global and European medical strategies.
• Ensure scientific and medical excellence by guiding the MSL team strategy and execution, including oversight of external service providers.
• Lead advocacy efforts to support appropriate brand adoption and ensure impactful scientific communication.
• Build and maintain strong relationships with key opinion leaders and medical experts across Germany.
• Collaborate closely with the Medical Director to establish a strong medical presence in Germany and support activities in Austria and Switzerland as needed.
• Foster close cross-functional collaboration between medical, sales, clinical, and brand teams, as well as with global and European medical affairs and clinical operations.
• Provide strategic and operational leadership for pre-launch and pre-reimbursement activities across all oncology compounds and indications.
• Secure and manage externally sponsored research projects to generate real-world evidence (RWE), including successful global funding acquisition.
• Offer medical expertise in regulatory and reimbursement processes and ensure compliance with pharmacovigilance and risk management requirements.
• Uphold legal and ethical standards in all medical activities in accordance with SOPs and local / EU regulations.

Qualifications & Experience