Required Competencies & Skills
Key information
- Publication date:16 October 2025
- Workload:100%
- Contract type:Unlimited employment
- Place of work:Pratteln
Santhera Pharmaceuticals is a Swiss specialty pharmaceutical company focused on medical science and the development and commercialization of innovative pharmaceutical products for the treatment of rare neuromuscular diseases with high unmet medical need. For further information, please visit the Company's website www.santhera.com Come and join our team to contribute to providing treatment options for patients with rare diseases that have a severe impact on the lives of affected children and adults. You can make a difference as:
Medical Affairs Director EU & ROW Location: Pratteln, Switzerland (Hybrid) Scope of Work
Reporting to the Global Head of Medical Affairs, the Medical Affairs Director EU & ROW is part of the CMO (Chief Medical Officer) organization and works closely with Clinical Development, Pharmacovigilance, Regulatory Affairs, Market Access, Marketing, and Country Medical Directors. The position supports the development and delivery of a robust medical strategy, including scientific exchange, data generation, publications, insights, and thought leader engagement, ensuring all activities uphold the highest standards of compliance and ethics. As a key member of the global medical team, the role fosters a collaborative, knowledgesharing culture across regions and functions. Key Responsibilities
Medical Affairs Director EU & ROW Location: Pratteln, Switzerland (Hybrid) Scope of Work
Reporting to the Global Head of Medical Affairs, the Medical Affairs Director EU & ROW is part of the CMO (Chief Medical Officer) organization and works closely with Clinical Development, Pharmacovigilance, Regulatory Affairs, Market Access, Marketing, and Country Medical Directors. The position supports the development and delivery of a robust medical strategy, including scientific exchange, data generation, publications, insights, and thought leader engagement, ensuring all activities uphold the highest standards of compliance and ethics. As a key member of the global medical team, the role fosters a collaborative, knowledgesharing culture across regions and functions. Key Responsibilities
- Support the Head of Medical Affairs in developing and executing the global medical affairs strategy for current and future pipeline indications.
- Focus strategy and activities on the key medical affairs pillars: (i) Scientific Exchange (ii) Data Generation (iii)
- Represent the company as a key clinical expert with medical and patient associations, and collaborate with commercial, market access, and affiliate medical teams to align global and local strategies.
- Lead and implement medical education events, training programs, and manage medical/scientific content for internal and external stakeholders.
- Oversee medical governance and compliance, including MLR process support, material review and approval in
- Provide medical expertise for product evaluations, benefit assessments, and support local launch needs; manage budget and resource allocation in consultation with the Head of Medical Affairs.
- Develop and manage Key Opinion Leader networks, ensure medical representation in external organizations, and act as a professional, compliant, and goal-driven collaborator.
- Accredited physician or registered pharmacist with a specialty degree or several years' experience in neuromuscular diseases; or Life Science graduate with a higher degree (MSc, MBA, PhD, or similar).
- Minimum 8 years of medical affairs experience in the pharmaceutical industry, ideally within the therapeutic area.
- 3+ years of line management and leadership experience.
- Proven track record in producing research publications (posters, presentations, and papers) and in supporting
- Prior experience as medical reviewer/approver in VEEVA.
- Experience in design, planning, and conduct of clinical research protocols is a plus.
- Knowledge and experience in Drug Safety, Regulatory, Health Economics, and/or statistical methods are a plus.
- Fluent English (spoken and written); strong ability and mandate to shape the external environment and partner effectively with internal stakeholders, especially Market Access and Marketing.
- Expert knowledge of the ABPI Code of Practice; recognised Thought Leader in compliance.
- Advanced understanding of ICH GCP.
- Strong people leader with proven team development skills.
- Advanced user of VEEVA and related systems.
- Skilled in publication and project management.
- Experienced in Thought Leader engagement and relationship management.
- Financially savvy, with solid budget management skills.
- Strong commercial mindset and strategic acumen.
