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ASAstrazeneca logo

Astrazeneca

Germany - Munich, Germany

Regional Medical Advisor Pipeline (Region Europe).

Introduction to role The Regional Medical Advisor Pipeline (RMAP) is a vital part of Global DR&S, serving as a field-based scientific resource responsible for the external scientific engagement (ESE) strategy for designated programs within a Therapeutic Area (TA) in their region. Collaborating closely with internal and external stakeholders, the RMAP will work on designated trials and cross-program scientific engagement needs. The RMAP will establish and maintain relationships with Key External Experts (KEEs) within a specific region to advise on Alexion’s clinical development strategy and trial execution within a TA. Reporting directly to the Global TA Head of External Scientific Engagement for Hematology, Nephrology & Transplants (HNT), the RMAP will play a crucial role in ensuring the successful performance of clinical trials, supporting activities such as early insight collection, guiding feasibility, and enhancing trial recruitment and retention. Accountabilities/Responsibilities KEE Partnerships Establishing long term partnerships with Key Experts Clinical Trial Support Inform identification of potential sites and investigators for clinical trials Drive scientific engagement initiatives to enhance recruitment and retention Scientific Exchange Develop and maintain the highest scientific and medical and scientific expertise in the relevant fields and be acknowledged internally and externally as an expert & resource in the assigned therapeutic area Lead & implement relevant local initiatives with key experts that could support R&D or study implementation (Scientific Panels, Advisory Board, Investigators as speakers, Lead local consensus) in alignment with GPT, Global R&D, COM and Country Medical Affairs colleagues Identify and address relevant educational gaps and relay those to Global Clinical Development Ensure timely and informative scientific/medical exchanges with trialists and internal partners, in accordance with compliance policies and with legal requirements Scientific Development Intelligence Develop in depth knowledge of the assigned therapeutic areas and pipeline assets Gather and effectively share actionable insights from the field with relevant stakeholders. Compliance Stay current of local laws and guidelines, codes of practices and Alexion policies relevant to Clinical Development and Medical Affairs activities Strong collaboration with (but not limited to): External Scientific Engagement Head Pipeline (EHP) & TA ESE Head Country Operations Medical Affairs Global Clinical Operations Clinical Development Market Access Launch excellence Essential Skills/Experience Bachelor’s degree in health sciences or equivalent Minimum 5 years of combined experience in Medical Affairs and Clinical Development Experience and skills in experts engagement and leading Advisory Boards Understanding of the healthcare landscape Willingness to travel up to 30% of time Fluency in English, both written and spoken Desirable Skills/Experience Advanced degrees (MD, PharmD, or PhD) in natural sciences. Expertise in Nephrology and/or Renal Transplant. Demonstrated patient-centric approach. Excellent communication and leadership skills Ability to build networks and manage complex projects. Independent, proactive work style with a team-oriented mindset. Adaptability and a positive outlook in challenging scenarios. Date Posted 30-Sep-2026 Closing Date Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact accommodations@Alexion.com. Alexion participates in E-Verify. For over three decades, patients and their caregivers have been at the center of everything we do. Every day, we are inspired to follow the science and think differently to create better outcomes for them and their families. Our mission is driven by understanding who they are as unique individuals, not solely defined by their diseases. We’re a leading rare disease company with a diversified projects. Our pioneering legacy in rare diseases is rooted in being the first to translate the complex biology of the complement system into transformative medicines over the past three decades. Today, we continue to push the boundaries of science and deepen our understanding of rare diseases with patient-centricity at the core. This knowledge allows us to innovate and evolve into new areas where needs are unmet and provide an opportunity to help people fully live their best lives.
Pay
Not stated
Where
Germany - Munich, Germany
Work
Not stated
Type
Not stated
Posted
30 Sep, 2026
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