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Interim Director Medical Affairs
vor 6 Stunden
Interim Director Medical Affairs
Start:
asap
Workload:
100
%
Duration:
9-12 months
Location:
Zug, Switzerland
About the Opportunity
We are supporting our client, an international biopharmaceutical company, in the search for an experienced Interim Director Medical Affairs. In this senior role, you will act as a subject matter expert within Medical Affairs and play a pivotal part in shaping and executing global and regional medical strategies. You will collaborate closely with Global and European Medical Affairs teams, ensure scientific and strategic excellence, and contribute to key medical deliverables including publications, scientific communications, and internal training materials.
The Interim Director will build and maintain strong relationships with leading external experts and academic institutions, representing Medical Affairs at advisory boards, scientific congresses, and investigator meetings. You will also work cross‑functionally to support pre‑launch and launch activities for late‑stage cardiovascular assets.
Key Responsibilities
Medical Leadership & Launch Support
- Drive Medical Affairs contributions to the launch of late‑stage cardiovascular compounds.
- Implement the regional Plan of Action aligned with Global and European Medical Affairs strategies.
- Lead medical pre‑launch and launch activities across Europe.
- Educate cardiovascular HCPs (heart failure and hypertrophic cardiomyopathy) on clinical profiles and therapeutic positioning.
- Engage in scientific exchange with KOLs, demonstrating deep understanding of mechanisms of action and clinical development (Phase I–IV).
Cross‑Functional Collaboration
- Provide day‑to‑day medical guidance and collaborate with Medical Affairs colleagues, country leadership, cross‑functional teams, and external partners.
- Contribute to congress strategy, advisory boards, field force training, medical information review, HEOR analyses, and policy‑related initiatives.
- Represent the company at scientific congresses, ensuring session coverage and booth support.
- Engage with patient groups and associations.
- Support publication strategy and review abstracts, posters, and manuscripts.
- Participate in cross‑functional European Medical and Commercial teams to inform brand strategy.
- Collaborate with Global & European Medical Affairs and R&D to maintain up‑to‑date product expertise.
- Provide input on medical education, grants, sponsorships, and responses to HCP inquiries.
Medical Governance
- Serve as a medical reviewer on the Medical Review Committee and the Promotional Materials Review Committee.
Data Generation & Scientific Exchange
- Present data at advisory boards and internal training programs.
- Partner with R&D and HEOR on data generation to address regional evidence gaps.
- Identify and engage opinion leaders to support scientific exchange.
- Collaborate with Market Access and HEOR on real‑world evidence and cost‑effectiveness study design.
- Support field medical teams and development of reactive materials.
- Participate in review and adjudication of investigator‑sponsored research proposals for Phase 4 programs.
Qualifications
- MD/MBBS with extensive Medical Affairs experience; cardiovascular expertise strongly preferred.
- At least 7 years of pharmaceutical industry experience, ideally at Director level.
- Proven Medical Affairs experience in Europe, including involvement in approvals, peri‑launch, and launch activities.
- Background in academic medicine, clinical research, study design, biostatistics, or epidemiology is desirable.
- Strong analytical, verbal, and written communication skills; excellent presenter.
- Familiarity with regional regulatory requirements and interactions with health authorities.
- Ability to think strategically about scientific communication and medical content.
- Additional European language skills beyond English are an advantage.
- Proficiency in Microsoft Office.
- Willingness to travel across Europe and internationally (approx. 35%).