Medical Manager METAP & CIS
Skills
About This Role
Primary Job Function
Developing medical strategies, managing external experts, and overseeing scientific communication and evidence generation for biosimilar products.
Key responsibilities
involve engagement with cross-functional teams internally, and engagement of KOLs, medical societies & Patient Advocacy Groups Externally, while ensuring the scientific and medical integrity of the product throughout its lifecycle
As MEAP, Turkey & CIS Medical Manager, you will lead the development and execution of strategic medical plans to support Abbott’s Biosimilars portfolio in key indications across the region.
This role is central to shaping clinical practice by providing deep technical expertise and generating relevant customer insights that drive advocacy and adoption of our biologic solutions.
You will collaborate closely with global, regional, and affiliate teams to ensure cross-functional alignment and maximize the value and impact of our biosimilar portfolio.
As part of the regional medical team, you will work to improve patient outcomes, elevate scientific engagement, and position Abbott as a trusted Healthcare Partner in Biosimilars across MEAP, Turkey & CIS region.
Key Responsibilities
- Strategic Medical Planning : Develop regional medical strategies, align cross-functionally, and adapt to market dynamics.
- External Engagement : Build relationships with KOLs, medical societies, and patient groups; lead advisory boards and consensus initiatives.
- Evidence Generation : Identify evidence gaps, support clinical research, manage IIS proposals, and ensure publication of studies.
- Affiliate Support : Guide affiliates through pre-launch, launch, and post-launch phases; deliver medical training.
- Brand Differentiation : Provide insights to commercial teams; adapt global positioning for regional markets.
- Medico-Marketing Programs : Execute medical education, expert meetings, PSP, and NPP programs.
- Medical Governance : Ensure compliance with internal policies and regulations in all medical activities.
Minimum Education/Qualifications Required
- Bachelor's degree in Medicine, preferably in the field of Oncology.
- Master’s degree/post graduate studies in Oncology and/or immunology is a plus.
Minimum Experience Required
- Minimum 5 years of medical affairs experience in pharmaceutical industry in immunology and/or oncology TAs at above country level
- Vast knowledge of the pharmaceutical environment across the region.
- Experience with launching of biologic molecules
- Experience in Clinical Research Programs
- Experience in comparative Analytical Studies
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