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Responsible for planning and executing medical activities and make sure timely and effective execution aligned to medical strategy. Reporting into Head of Rare Disease Medical, Japan.
Responsabilités:
Lead to propose and create his / her responsible parts in annual Japan Medical plan and execute as a representative leader in Medical
Provide medical and technical input into medically accurate development of Brand promotional materials in close align with marketing team
Work with cross-functional, multidisciplinary teams to facilitate the creation of medical strategies about products to answer unsolicited medical requests from internal and external stakeholders
Leverage (unmet) medical needs in order to support lifecycle opportunities based on patient needs on a rolling basis through the development cycle
Liaise with key internal stakeholders to help develop, secure approval for and implement independent post approval studies that have the potential to support lysosomal disease related products
Actively engage regional thought leaders, investigators and potential investigators in two-way scientific communication around ISS/phase IV studies
Ensure timely review, approval and support as appropriate for ISSs
Advise on locally driven early stage clinical trial plans
Lead Publication strategy planning and its execution. Lead activities related article publications, presentations at congresses and symposia
Establish and maintain contact with Key Opinions Leaders (KOLs) with high level scientific and business communication skills
Lead to shape field strategies in align with global medical director group and local MSLs
Develop and maintain scientific relationships with TLs to create awareness and understanding of the therapeutic area and products, and facilitate scientific exchange with KOLs
Present data at and chair as a leader for TA Medical Advisory Boards
Develop and leverage medical/scientific insights through attendance at scientific meetings to further develop own knowledge base in line with company and medical strategy
Conduct/attend/present at Advisory Boards initiated by the affiliate organization if there is a clear need for specific medical input
Support Global Rare Disease Sample Testing Program to maintain the proper use of our compounds
Exigences:
Advanced degree in life science field (MD/PhD/PharmD)
Minimum 3 years of experience in a pharmaceutical company in either RD (Research & Development) or MA (Medical Affairs)
Scientific expertise
Professional communication skills
Deep understanding and knowledge of local regulations and codes of practice for pharmaceutical industry
Knowledge of relevant healthcare systems, the evolving medical landscape, regulatory and payer environment, public health and industry trends
Business level English
Native level Japanese
Ce que nous offrons:
Equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity
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