Radiprodil Global Medical Ass Director

MAIN RESPONSIBILITIES:

As a key member of the Medical Affairs organization and cross ‑ functional teams, the Global Medical Lead serves as the scientific expert, strategic partner, and medical ambassador for the GRIN ‑ NDD therapeutic area. This role drives science ‑ based decision ‑ making, advances medical understanding in collaboration with healthcare professionals and external stakeholders, and supports the evolution of diagnosis and treatment paradigms.

Strategic Leadership and Medical Planning

• Enable, partner, and co‑create the global strategy for radiprodil throughout its lifecycle.
• Develop the global medical plan and guide/enable countries in the creation and execution of their local medical plans.
• Develop and update strategic scientific documents aligned with franchise priorities, including scientific narratives, slide decks, and core medical materials.

Execution of Global Medical Activities

• Ensure excellence and timely execution of medical tactics, including data and evidence generation, scientific exchange, and stakeholder engagement activities (e.g., advisory boards, congress symposia, publication planning).
• Approve non‑promotional and promotional materials, ensuring accuracy, appropriate interpretation, and compliance with global requirements.

• Build and maintain strong relationships with key opinion leaders, principal investigators, and other external experts.
• Represent the company at major scientific meetings, conferences, and congresses.
• Maintain deep clinical and scientific expertise in the assigned product, therapeutic area, and competitive landscape, and provide medical guidance to colleagues globally and locally.
• Support other medical activities as assigned to advance the therapeutic area and company objectives.

Scientific Insight Generation and Cross‑Functional Collaboration

• Participate in the collection, interpretation, and exchange of scientific insights relevant to the company’s strategy and development efforts.
• Collaborate closely with cross‑functional teams to ensure alignment between medical strategy, evidence generation, and broader organizational objectives.
• Contribute to internal scientific training and knowledge‑sharing initiatives.

DESIRED PROFILE

Qualifications and Experience

• Advanced scientific degree (MD, PharmD, PhD, MSc) preferred; life sciences degree required. MD preferred
• > 8 years’ experience in Medical Affairs.
• Global or international experience and proven track record in drug launches required.
• Experience in rare diseases within brain health highly preferred.
• Previous field medical experience (e.g., MSL,) highly preferred.
• Experience in real‑world evidence generation, publications, and scientific presentations at congresses or academic forums.

Skills, Competencies and Mindset

• Demonstrated ability to drive results aligned with company objectives and values.
• Strong analytical and problem‑solving skills, with the ability to interpret complex scientific data.
• Ability to work effectively in a cross‑functional/franchise environment.
• Proven ability to build and maintain trusted relationships with thought leaders through scientific expertise and reliable follow‑through.
• Strong leadership skills with the ability to synthesize and communicate information clearly to diverse audiences.
• Excellent communication, facilitation, and presentation skills.

• Passion for science and innovation, with a patient centric approach and a genuine motivation to help people.
• Ability to simplify complex scientific concepts into clear, engaging, and accessible materials.
• Strong project management capabilities, with the ability to manage multiple priorities and stakeholders under time and budget constraints.

Initial Salary: 64.000€

Angelini Pharma is an Equal Opportunity Employer.

We believe that diversity is a huge value that contributes to individual and company success. We are committed to create and foster a diverse and inclusive environment.