Medical Director UK & Ireland

Who We Are
BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.
Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.
Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.
About Worldwide Research and Development
From research and discovery to post-market clinical development, our R&D engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with rare diseases.
Medical Director UK and Ireland
Roles and Responsibilities:
• Lead Medical Affairs activities in the assigned indications
• Define and implement the medical strategy according to the company's orientations, and for the entire product portfolio developed by BioMarin
• Oversee and lead the Medical Affairs activities in the UK & Ireland
• Coordinate Medical Affairs activities to ensure the successful implementation of Action Plans and support BioMarin clinical development activities.
• Develop and deliver scientific and medical information to answer specific and documented questions from Healthcare Professionals (HCPs).
• Lead the Medical Affairs team developing and maintaining the expertise of all members of the Medical Affairs Team for the therapeutic areas covered BioMarin
• Contribute to the development of knowledge of the relevant products and pathologies, externally and internally.
• Ensure compliance of Medical Affairs activities to BioMarin policies and procedures, as well as all local regulatory and legal requirements. Ensure that appropriate systems and SOP/processes are being followed to meet these requirements.
• Interact and optimise relationships with Thought Leaders and other members of the medical community to assist in understanding current disease management issues and data gaps in BioMarin areas of interest
• Encourage appropriate research collaborations with academic institutions in predefined Areas of Research Interests.
• Participate as an active and integral member of the region management team
Medical strategy:
• Define, develop, oversee, and effectively implement the country medical strategies for products already marketed and for investigational agents in development.
• Represent country interests to the Global and International medical teams to guide the long term strategy of the product portfolio.
• Be the preferred scientific and medical contact with external thought leaders, Patient Associations and National Regulatory authorities;
• Provide advice and scientific assistance to General Manager and other functions of BioMarin
• Under the supervision of the General Manager, and in collaboration with the Market Access department and regulatory affairs contribute to the development of National Reimbursement applications.
• Partner effectively with Country Medical Directors in the EUCAN region to contribute to overall International and Global Medical Strategy
Clinical research:
• Define and implement, in conjunction with health authorities, risk management plans, Phase IV studies and cohort follow-up studies for registered products while ensuring compliance with the Company's ethics and interests.
• Contribute to the development of public-private partnerships or research partnerships, including coordinating the implementation of studies led by an external investigator (Investigator Initiated Studies).
Medical affairs:
• Participate in scientific events, national or international congresses, meetings organized by learned societies or foundations.
• Ensure compliance with country regulations for all oral and written scientific communications on products and their environment;
• Develop scientific projects, patient support programs, medical education programs and clinical studies in collaboration with experts in the diseases covered by BioMarin gathered within Advisory Boards
• Respond promptly to requests for scientific and medical training;
• Where appropriate, write the medical part of the files for Regulatory Authorities, or any other Health Authority
Medical governance:
• Contribute to the drafting and implementation of procedures that govern the activities of the Medical Team;
• Comply with, and enforce, regulatory obligations;
• Comply with, and enforce, BioMarin regulatory obligations and procedures or scientific and medical information in response to HCP requests.
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