Senior Manager/Associate Director, External Programs, Global Medical Affairs

Senior Manager/Associate Director, External Programs, Global Medical Affairs

Ascendis Pharma

Hellerup, Denmark

We are seeking a passionate Senior Manager/Associate Director (dependent on experience) to join our growing team. As a key member of the Ascendis Pharma team, you will play a crucial role in the development and execution of our external programs across the endocrine portfolio at an above-country level. This includes overseeing various projects and initiatives, such as evidence generation management, early access program management, patient advocacy, and more.

You will work closely with the rest of the Global Medical Affairs Strategy department to align on the development and execution of the overall Medical Affairs Strategy.

You will join the Global Medical Affairs team, which consists of 30 colleagues across the US and Europe, and report directly to Anne Mette Beier, Global Medical Director for External Programs, who is based in Hellerup, Denmark. You will be based in the Hellerup office.

Your key responsibilities will include:

  • Execute Early Access Program planning: Manage all aspects of EAPs, applying risk management principles;
  • Coordinate with cross-functional teams: Align on strategic priorities spanning Clinical, Regulatory, Commercial, and Marketing areas;
  • Strategic operational planning: Develop efficient plans within budget, integrating external resources;
  • Direct complex project management: Lead projects to deliver high-quality outcomes;
  • Represent the company externally: Attend meetings to enhance visibility and build relationships;
  • Collaborate internally on business initiatives: Define projects that support company goals;
  • Ensure compliance: Uphold SOPs and regulatory standards in all activities.

Qualifications and skills:

You hold a relevant academic degree, preferably a Master of Science, and have 4–7 years of experience in project management within medical affairs, clinical operations, or a related field within the pharmaceutical or biotechnology industry.

Knowledge of relevant therapeutic areas and disease states is preferred.

Additionally, you have:

  • A proven track record of successfully managing external programs and collaborations with healthcare professionals and other stakeholders;
  • A strong understanding of medical science, clinical research methodologies, and related areas;
  • The ability to interpret and articulate clinical/HEOR data and its impact on clinical development and commercial programs;
  • In-depth knowledge of compliance and regulatory requirements for pharmaceutical Medical Affairs, R&D, and Commercial activities.

Key competencies:

You are a strong team player, analytical, and have a can-do attitude. You possess an entrepreneurial mindset and can thrive in an informal, open environment where innovation and change are key.

The ideal candidate has excellent project management skills combined with outstanding stakeholder management abilities. To succeed in this role, you should also possess the ability to lead strategically, drive performance, build alignment, inform, negotiate, and collaborate across partnerships with strong written and verbal communication skills.

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