About The Position
The Regional Medical Advisor Pipeline Director (RMAP), is a vital part of Global DRS, 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, as well as collaborate on the cross-program scientific engagement needs for the TA. 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, 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.
Requirements
- Bachelor’s degree in health sciences or equivalent
- Minimum 7 years of combined Medical Affairs, Clinical Development and/or relevant clinical experience.
- Experience and skills in experts' engagement and leading Advisory Boards
- Understanding of the healthcare landscape
- Willingness to travel up to 50% of time
- Fluency in English, both written and spoken
Nice To Haves
- Advanced degrees (MD, PharmD, or PhD) in natural sciences.
- 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.
Responsibilities
- Regional ESE Strategy Primary responsible for the overall scientific engagement (ESE) strategy within a Therapeutic Area (TA) in their region.
- 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 to support DRS objectives or successful study implementation in alignment with Global Program Teams, 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.
- Team efficiency Leads and optimizes ESE processes end‑to-end, identifying gaps, standardizing best practices, and driving measurable efficiency gains across teams. Proactively scopes, prioritizes, and steers non‑rMAP initiatives with cross‑functional stakeholders, balancing portfolio needs and ensuring strategic impact and adoption.
- Compliance Stay current of local laws and guidelines, codes of practices and Alexion policies relevant to Clinical Development and Medical Affairs activities.
Benefits
- Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
