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Immunology Medical Lead

2 semanas atrás

Lisboa, Lisboa, Portugal Allergan Tempo inteiro

Role Summary
The Senior Medical Manager for Immunology will be responsible for leading and managing the Immunology Medical Team. This includes defining and executing medical affairs strategies for our affiliate in the Therapeutic Area, ensuring effective implementation of company strategy, and providing strategic medical affairs support to cross-functional partners.

Key Responsibilities
- Define and execute medical affairs strategies for the Affiliate in the Therapeutic Area under their responsibility
- Lead and manage the Medical Team (Medical Managers, Medical Advisors, Medical Liaisons and Contractors) who are specifically dedicated to the Therapeutic Areas and the brands
- Ensure the effective implementation of the Company/Affiliate strategy for the TAs/Brands under their responsibility
- Provide strategic medical affairs support to cross-functional affiliate partners in the Therapeutic Area under their responsibility
- Develop and maintain professional and credible relationships with external experts and academic centers
- Identify appropriately qualified external local experts who would wish to engage in collaborative efforts with AbbVie
- Ensure a high level of scientific integrity in these collaborative efforts
- Collaborate with CCOM to identify and prioritize Development Studies for the Affiliate
- Ensure achievement of Medical Affairs objectives in the context of the 1R&D partnership

Requirements
- Medical Degree or Equivalent scientific background in pharmaceutical or chemistry sciences
- Previous medical affairs pharmaceutical or biopharmaceutical industry experience is essential, and management experience of medical teams & significant numbers of medical/scientific staff for 5 years (minimum) is expected
- Demonstrated ability to lead a medical team and to work across different Diseases/TAs
- Broad and demonstrated understanding of drug development and commercialization processes, sound and current knowledge of the regulatory environment, significant experience in overseeing or conducting clinical trials, solid understanding of trial design and methodology, and understanding of the need to balance safety and efficacy concerns