Regional Medical Advisor

il y a 1 semaine

Bruxelles, Région de Bruxelles, Belgique Amicus Therapeutics Temps plein

Job Brief:

Regional Medical Advisor (BeNeLux)

Amicus Therapeutics is a global, patient-dedicated biotechnology company focused on discovering, developing, and delivering high-quality medicines for people living with rare metabolic diseases.
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Position Summary


The Regional Medical Advisor (RMA) will work as a member of the France-Benelux Medical team to support the Amicus portfolio with products in different phases of lifecycle and relay field-based clinical/medical insights back to Amicus to impact the future strategy so Amicus can continue to bring innovative medicines to patients with rare diseases.

Under the leadership of the France Benelux Senior Country Medical Director, the RMA will be accountable for the planning and execution of the Medical affairs plans in Benelux countries.

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Roles and Responsibilities:***- Based on the Senior Country Medical Directors advice and in close Medical Team and cross-functional alignment, the RMA will help to define the Medical Affairs strategy for the Benelux countries according to the Strategic Imperatives defined at the Global level and will execute the medical plans for all Amicus products.

  • Responsible for activities related to Medical Information and Communication, Medical Education and Training, Investigator Initiated Trials and Key Opinion Leader outreach bringing value via scientific exchange.
  • Provide Research & Clinical Development support as needed.
  • Under the leadership of the Senior Country Medical Director, RMA will represent Amicus in scientific presentations, conferences, and will support the Commercial Organization while ensuring compliance with all Amicus policies and procedures as well as local regulatory and legal requirements.
***- Oversee aspects of Medical Affairs for Benelux including medical support of product launches, thought leader identification and network development in the field of Lysosomal disorders

  • Serve as the primary Amicus external Medical Affairs representative for assigned key stakeholders, establish oneself as a reliable, trusted, resource of accurate, uptodate, medical and scientific knowledge providing deep and advanced disease state and product information, as well as facilitating collaborations aligning with Amicus' strategic goals
  • Develop strategic and tactical operational plans including Key Opinion Leader (KOL) engagement and considering insights from KOLs
  • Systematically identify and develop new as well as maintain and enhance existing scientific collaboration and exchange with external physicians, genetic counselors, nurses, pharmacists, scientific experts, hospital teams, educators, and investigators in Benelux countries and current therapeutic areas
  • Organize standalones, satellite symposia, local publications, medical education, and Advisory Boards
  • Develop various scientific projects, patient support programs, medical education programs in collaboration with experts in the diseases covered by Amicus gathered within Advisory Boards
  • Attend congresses and be the medical point of contact on the booths to answer requests for scientific and medical information from healthcare professionals
  • Attend appropriate scientific meetings, engage in continuous learning within the therapeutic areas, and communicate regularly internally to ensure that the entire France & Benelux Medical Team benefits from individual learning
  • Partner and collaborate with Amicus Patient and Professional Advocacy (P&PA) in developing and maintaining partnerships with advocacy groups across therapeutic areas
  • Work with members of the commercial team to communicate science and clinical trial results objectively and accurately in a fair and balanced manner
  • Provide medical support in crossfunctional projects (e.g., diagnostic initiatives, informational material, local scientific publication)
  • Provide regular and documented literature reviews to maintain medical knowledge;
  • Manage the process of educational grant requests and IIP (Investigatorinitiated Program) activities according to the internal areas of scientific interest
  • Provide ongoing disease and product training to field personnel
  • Reply orally, in writing or in person to any request for scientific information from healthcare professionals or patients, based on the reply supporting documents prepared by Global Medical Information, and document the replies
  • Consistently collect, report, and represent clinical insights and unanswered questions received from external contacts to the appropriate channels internally
  • Seek clarification from management and/or Compliance & Legal when uncertain whether a proposed activity could violate Amicus policy or the law
  • The RMA role entails not only scientific and customer expertise, but also requires the ability to understand and effectively utilize approved resources to fulfill administrative, procedural, and legal requirements to address the customer needs. These activities may include proficiency in co

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