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For our client, the international Headquarter of an innovative, growing pharmaceutical company based in Zug/Switzerland, we are looking for an interim

Associate Director International Medical Affairs - Allergology, Hematology, Oncology 80% - 100% (Ref. Nr. 2730)
10 months temporary contract – immediately available

The Associate Director, International Medical Affairs will be reporting to the VP Head of International Medical Affairs and will support Medical Affairs operations, scientific communication, and cross‑functional projects across multiple therapeutic areas. You will collaborate closely with internal stakeholders in Medical, Clinical Development, Regulatory Affairs, Commercial, and Country Teams, as well as with external scientific experts and healthcare professionals. This position offers the opportunity to contribute to impactful medical projects in a dynamic and highly collaborative environment.

Your main tasks

• Support Medical Affairs programs, scientific activities, and operational processes while ensuring full compliance with regulatory and internal standards.

• Contribute to medical education initiatives, congress activities, symposia, and scientific communication efforts.

• Align medical strategies and tactics with broader cross‑functional plans, including communications and commercial objectives.

• Support Life Cycle Management (LCM) projects and act as an international liaison for R&D‑related development activities.

• Build relationships with healthcare providers, KOLs, investigators, and external partners to support scientific engagement.

• Collaborate with Clinical Development and Clinical Operations teams to review and support clinical programs and investigator‑initiated studies.

• Maintain up‑to‑date scientific knowledge and contribute to scientific training, advisory boards, internal meetings, and congress participation.

Your profile

• Advanced scientific degree (PhD, MD) with solid experience in Medical Affairs within the biopharmaceutical industry.

• Demonstrated cross‑functional project management experience in complex matrix environments.

• Strong understanding of the drug development process, medical frameworks, and requirements across Allergology, Hematology and Oncology (regulatory, HTA, Early Access Program, and RCT requirements).

• Excellent scientific communication skills with the ability to translate data into clear, impactful insights.

• Experience supporting product launches and collaborating with global or regional medical and commercial teams.

• High level of emotional intelligence, resilience, and the ability to manage complexity and shifting priorities.

• Fluent in English, with strong presentation, stakeholder management, and decision‑making capabilities.