Beschreibung

In this role, you will shape the medical affairs strategy for the EUR region, collaborating with various teams to ensure scientific alignment and compliance. You will engage with key opinion leaders and healthcare professionals, delivering impactful presentations and fostering partnerships while leading a dedicated team.

Anforderungen

• •MD, PhD, or PharmD
• •Minimum 10 years of experience in medical affairs or clinical development
• •Extensive experience in biotech or pharmaceutical industry, particularly in rare diseases or neurology
• •Excellent communication, presentation, and relationship-building skills
• •Proven track record in leading medical affairs strategies and teams or clinical studies at a regional level
• •Strong knowledge of European healthcare landscape and regulatory environment
• •Ability to build effective professional relationships across functional areas
• •Experience in a matrix, cross-functional environment; excellent collaboration skills
• •Ability to work effectively in a fast-paced, innovative environment
• •Outstanding work ethic and integrity
• •Strong interpersonal skills, particularly motivational and negotiation skills
• •Fluency in English; proficiency in additional European languages
• •Ability to travel across Europe as needed

Aufgaben

• •Lead the development and execution of the EMEA medical affairs strategy
• •Provide medical insights for business and regulatory decisions
• •Collaborate with cross-functional teams to ensure scientific alignment
• •Develop medical strategy and content for congresses and advisory boards
• •Disseminate accurate and scientifically sound medical information
• •Lead the creation of region-specific scientific publications and presentations
• •Deliver scientific presentations to diverse audiences
• •Represent the company at key scientific and medical conferences
• •Develop and maintain relationships with regional KOLs and HCPs
• •Engage with external experts to gather insights and strengthen partnerships
• •Support the development and approval of promotional materials
• •Provide medical support for clinical development and research in Europe
• •Assess medical education needs and develop educational strategies
• •Coordinate investigator-initiated studies with academic institutions
• •Ensure compliance with regulatory requirements and ethical guidelines
• •Support regulatory submissions and product launches
• •Lead and mentor a team of medical affairs professionals
• •Foster a culture of continuous learning within the medical affairs team