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Teva Associate Medical Director - Migraine EU 
Netherlands, North Holland, Haarlem 
377606710

17.09.2024

This role will be based in our European HQ in Haarlem.

The opportunity
  • Execution of all medical activities and projects for the migraine product.
  • Providing scientific/medical leadership, strategy, and support for Teva products in the migraine/CNS area.
  • Leading integrated strategic medical & brand planning, and execution of all medical activities and projects for the migraine product within Medical Affairs Europe, together with strategic partners in Commercial, HEOR, R&D, Regulatory, Market Access, Country Medical Departments & other x-functional partners.
  • Representing Medical Affairs Europe in strategic discussions regarding brand strategy, lifecycle management, business development, clinical research, RWE, and HEOR planning.
  • Development and execution of data generation projects, publications, posters, abstracts, manuscripts for the migraine/CNS area.
  • Providing necessary support and oversight to country teams via close collaboration and follow-up on a timely basis.
How you’ll spend your day
  • Serves as European Medical ‘point of contact’ for the product in the migraine area. Responsible for medical and scientific support to country medical teams, global and regional brand teams.
  • Development & execution of the regional strategic brand plans/medical plans and operating plans (medical elements), in collaboration with other cross-functional teams.
  • Development and coordination of the execution of the overall medical strategy for Teva’s migraine product in close collaboration with Country Medical Affairs teams.
  • Contributor and member of the regional brand team and when needed part of Global Matrix team as a representative of EU.
  • Support to clinical development with input on target product profile, based on European market access and health economics and outcomes research needs.
  • Provide oversight and support to execution of Global studies in Europe. Provide input to Phase II-III-IV studies design based on market access needs of European countries.
  • Collaboration with Global Scientific Communications including strategy development and writing and review of manuscripts, abstracts, and posters as part of the publication team.
  • Development and maintenance of professional relationships with external experts and professional medical and patient associations.
  • Serves as an internal medical expert for product and disease-related content, for all cross-functional teams and country teams as well as external stakeholders. Educate country medical teams about the products and therapy area.
  • Review and approval of promotional/non-promotional/educational/patient support materials at European regional level.
  • Leading RWE data generation strategy and execution in Europe via setting the strategy in collaboration with other internal and external stakeholders. Initiating the prospective/retrospective studies, protocol development, site selection, external vendor-CRO management, project management, budget management, patient recruitment and publication planning and execution.
  • Planning and execution of European medical congresses, satellite symposia, advisory board meetings, speaker trainings, round table meetings, medical congresses & medical educational booths at Europe level.
  • Review and approval of ISS proposals, company sponsored studies, collaborative research proposals in relevant internal committees.
Your experience and qualifications

We are looking for a Medical Doctor. Experience as a Neurologist will be a big plus.


You have solid accumulated experience (5+ years) working in the medical department within the pharmaceutical industry, experience in neurology is preferred.


Next to that you have experience in:

  • Launch planning and execution of new product launch in Medical Affairs.
  • Planning publication strategy, development, review and full execution of manuscripts, abstracts and posters.
  • Broad knowledge of drug development, designation of a clinical trial/ observational study, regulatory requirements and life cycle management.
  • RWE data generation strategy development and execution, protocol/clinical study report development, patient recruitment, development of publications, project management of RWE studies & ISS management.
  • Budget management
  • Preferably above country experience in Europe or Global Medical Teams.
Your competences and skills
  • Great interpersonal skills; strong team player with positive attitude, excellent collaboration, able to work with different cross functional teams effectively.
  • Strong execution skills, able to deliver in a fast pace environment.
  • Ability to work across different cultures, cultural awareness and sensitivity.
  • Experienced in developing strategy, planning and executing medical plans;
  • Ability to set direction and bring different matrix teams along with excellent interpersonal skills;
  • Must have excellent communication and presentation skills, verbal and written;
  • Strategic thinker and has a creative, solution-oriented style;
  • Flexible and able to work and execute in a fast-paced, rapidly changing environment on multiple projects with aggressive deadlines; team-oriented energetic and passionate about making a difference;
  • Has a strong work ethics and character is of the highest integrity, including strong ethical and scientific standards.
  • A good listener with diplomacy and positive influencing and negotiation skills
Reports To

Therapy Area Head - Europe

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