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MEMerck & Co., Inc.

Regional Director of Medical Affairs, Hematology (MER & EEMEA Region)(m/w/x)

Zürich
Full-timeOn-siteSenior

Executing scientific and medical plans for biopharmaceuticals at global manufacturer. M.D., Ph.D., or Pharm.D. with 5+ years oncology or blood disorder experience required. Work in global matrix environment with extensive cross-functional partnership.

Requirements

  • M.D., Ph.D. or Pharm.D.
  • At least 3 years' experience in medical and scientific affairs in EU5CAN, MER and/or EEMEA
  • Minimum of 5 years of Hematology and/or Oncology experience
  • Strong prioritization and decision-making skills
  • Ability to effectively collaborate with partners across divisions in a matrix environment
  • Excellent interpersonal, analytical, communication skills (written and oral) in addition to results-oriented project management skills
  • Hematology role experience (3+ years)
  • Customer expertise, especially scientific leadership and other key stakeholders in Hematology
  • Adaptability, Board of Directors Presentation, Clinical Development, Communication, Cross-Cultural Awareness, Data Analysis, Decision Making, Healthcare Education, Healthcare Marketing, Hemagglutination Assays, Hematology, Hemodialysis, Interpersonal Relationships, Interventional Oncology, Investigator-Initiated Studies (IIS), Medical Affairs, Medical Marketing Strategy, Medical Writing, Oncology, Pharmaceutical Medical Affairs, Prioritization, Program Implementation, Project Management, Scientific Communications

Tasks

  • Guide country research division colleagues in executing the annual scientific and medical affairs plan for Hematology
  • Chair the MER/EEMEA Regional Medical Affairs Team to develop and execute medical affairs strategies
  • Align scientific exchange with global and regional goals
  • Consolidate actionable medical insights from countries in the region
  • Partner with regional Commercial, Outcomes Research, Policy, and Market Access teams to drive regional plans
  • Engage with scientific leaders and key stakeholders about the company's emerging science
  • Support affiliates in engaging with national scientific leaders as a regional therapeutic area expert
  • Organize regional symposia and educational meetings
  • Facilitate regional expert input events to gather insights on new medicine development
  • Assist key countries in developing local data generation study concepts and protocols
  • Review investigator-initiated study proposals per established process
  • Manage regional programs to support the safe utilization of the company's medicines

Work Experience

  • 5 years

Education

  • Master's degree

Languages

  • EnglishBusiness Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Merck & Co., Inc. and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.

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