Position Summary
The (Senior) Medical Director, MSC will lead the development and execution of the Medical Affairs strategy for RETT syndrome in alignment with the Regional Medical Affairs strategy, collaborating closely with the field Medical Science Liaisons (MSLs). This role encompasses the creation of (pre)launch plans, along with local support and implementation of Managed Access and Patient Support activities, as appropriate, in select dedicated countries across Europe. The successful candidate will focus on building and maintaining external stakeholder relationships and collaborations, positioning Acadia as a thought leader and a valued partner within patient advocacy and the RETT medical communities in various smaller EU countries. This individual will also be responsible for ensuring the effectiveness and compliance of scientific exchanges to satisfy the needs of clinicians, patient advocates, and other key external and internal stakeholders.
Primary Responsibilities
- Manage specific geographical territories in mid-sized European countries, with the potential for additional markets based on experience, workload, and organizational needs as the company expands its footprint across Europe.
- Provide scientific and medical leadership through the development of strategic country medical affairs (pre)launch plans, identifying unmet medical needs and data gaps.
- Establish strategic partnerships with Centers of Excellence, Key Opinion Leaders (KOLs), and Patient Advocacy Groups (PAGs) in areas of scientific interest, working alongside local MSLs as required.
- Ensure cross-functional collaboration and input from key stakeholders to effectively manage relationships and ensure alignment with the medical strategy.
- Coordinate operational medical excellence in partnership with EU field medical teams to capture and track key medical tactics and prelaunch activities across these countries.
- Provide medical expertise and editorial support for disseminating data at conferences and in medical journals.
- Engage with key healthcare professionals (HCPs) in the exchange of scientific and medical information through Advisory Boards and presentations at national meetings and conferences.
- Develop and maintain professional relationships with Key Opinion Leaders and emerging scientific leaders in the community in collaboration with MSLs.
- Communicate insights gained regarding the competitive landscape, unmet needs of physicians and advocacy groups to cross-functional stakeholders, and develop actionable plans based on these local insights.
- Assist in publication activities, including the review and approval of abstracts and manuscripts, as well as the development of local publication strategies in collaboration with authors as needed.
- Gather and report field medical insights utilizing the existing iArt CRM system, in accordance with company rules and requirements.
- Understand the needs of HCPs across individual Medical Science Centers (MSCs) and support a strategic and tactical medical affairs plan focused on enhancing patient care and generating relevant evidence for RETT syndrome.
- Perform other duties as assigned.
Education/Experience/Skills
A qualified candidate will possess an MD (PhD, PharmD, or equivalent degrees may also be considered) with 10+ years of Medical Affairs experience within the pharmaceutical or biotech industry in Europe. Experience with rare (neurological) diseases in the European context is essential, along with a comprehensive understanding of the individual healthcare systems and regulations of various countries, including pre-approval and/or early access activities. Demonstrated expertise in HCP engagement and prior interaction with Patient Advocacy Groups, including the development of integrated communication strategies to enhance disease awareness, is crucial. An equivalent combination of relevant education and experience may also be considered.
Key Skills
- Extensive knowledge for critically appraising studies and clinical evidence, enabling engagement with HCPs on a high scientific level.
- In-depth understanding of compliance and regulatory requirements for pharmaceutical Medical Affairs, R&D, and Commercial activities across Europe.
- Excellent communication, collaboration, and presentation skills, with experience in delivering scientific presentations.
- An agile, independent, and proactive working style.
- A proven ability to build strong working relationships across functions and organizations.
- Ability to collaborate effectively and share information to contribute meaningfully to the planning process and execute the agreed local Medical (pre)launch plan in alignment with the Regional Medical Affairs strategy, alongside MSLs.
- Fluency in English (native level) is essential, with proficiency in additional languages being a significant advantage. Strong English communication skills, with the ability to articulate and present details clearly, are required.
- Willingness to travel both locally and internationally is required.
Apply online using the form below. Only applications matching the job profile will be considered.