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Associate Medical Director - Migraine Eu

5+ years
Not Disclosed
10 Nov. 21, 2024
Job Description
Job Type: Remote Education: B.Sc./M.Sc./M.Pharm/B.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Who We Are

Teva Pharmaceuticals is a global leader in the pharmaceutical industry and the world's largest producer of generic medicines. We are dedicated to improving health and expanding access to high-quality healthcare solutions worldwide. With operations in over 80 countries and a workforce delivering solutions to 200 million people daily, our diverse product portfolio and innovative pipeline reflect our patient-centered mission. Through continuous investment in research, development, marketing, and innovation, we strive to enable better, healthier lives.

Join us on this exciting journey of growth and innovation!


Location

  • Base: European Headquarters in Haarlem, Netherlands.
  • Travel Requirement: 20-30% to other EU locations.

The Opportunity

We are seeking a Medical Affairs Professional to lead and execute medical activities and strategies for Teva’s migraine product within the CNS therapeutic area. This role involves cross-functional collaboration, strategic medical planning, data generation, and leadership in supporting country teams and stakeholders.

Key Responsibilities

Strategic Medical Leadership
  • Serve as the European Medical point of contact for Teva’s migraine product, providing medical and scientific support to country medical teams, global, and regional brand teams.
  • Develop and execute regional strategic brand plans, medical plans, and operating plans in collaboration with cross-functional teams.
  • Contribute to lifecycle management, business development, clinical research, RWE, and HEOR planning.
Data Generation & Publications
  • Lead the development and execution of data generation projects, including manuscripts, posters, abstracts, and publications within the migraine/CNS area.
  • Provide input on the design of Phase II-III-IV and observational studies to align with market access needs of European countries.
  • Oversee Real-World Evidence (RWE) data generation strategy and execution, including study initiation, protocol development, site selection, vendor management, and publication planning.
Collaboration & Communication
  • Build and maintain professional relationships with external experts, patient associations, and medical societies.
  • Act as an internal medical expert for product and disease-related content, supporting cross-functional teams, stakeholders, and country teams.
  • Educate country medical teams about therapy areas and products.
Compliance & Regulatory Oversight
  • Review and approve promotional, non-promotional, educational, and patient support materials at the European regional level, ensuring adherence to regulations.
  • Provide oversight and support for compliance processes, study protocols, and submissions.
Event Management
  • Plan and execute medical congresses, satellite symposia, advisory board meetings, speaker training, roundtable meetings, and educational booths across Europe.

Your Profile

Qualifications

  • Medical Doctor (Neurology experience preferred).
  • Minimum of 5 years of pharmaceutical industry experience in a medical role, preferably within neurology/CNS.

Skills & Experience

  • Proven experience in:
    • Product launch planning and execution in Medical Affairs.
    • Publication strategy, including development and review of manuscripts, abstracts, and posters.
    • Drug development, clinical trial design, and lifecycle management.
    • Real-World Evidence (RWE) strategy and execution.
    • Budget management.
    • Cross-functional collaboration in European or global medical teams.
  • Strong knowledge of regulatory requirements and compliance standards.

Competencies

  • Strong interpersonal and team collaboration skills with a positive, solution-oriented approach.
  • Strategic thinker with excellent execution and multitasking abilities.
  • Effective communicator with excellent verbal and written presentation skills.
  • High ethical and scientific integrity.
  • Flexible and adaptable in a fast-paced environment with tight deadlines.

Why Join Us?

  • Be part of a dynamic, innovative, and patient-centered organization.
  • Work on impactful projects with opportunities for growth and development.
  • Collaborate with diverse, cross-functional teams across Europe.

Reporting Line

Reports to the Therapy Area Head - Europe.


For Current Employees

If you’re already part of Teva, apply through the Internal Career Site available on "Employee Central" for priority consideration. Contact your local HR/IT partner if you encounter issues.


Equal Employment Opportunity Commitment

Teva Pharmaceuticals is an equal-opportunity employer dedicated to fostering a diverse and inclusive workplace. We accommodate all candidates throughout the recruitment process to ensure a positive experience.

Join Teva and make a difference in healthcare!