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Merck & Co., Inc.
19d ago

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

Zürich
Full-timeOn-siteSenior

Description

In this role, you will lead the execution of medical affairs strategies in Hematology across the MER and EEMEA regions, collaborating with cross-functional teams and engaging with scientific leaders to drive impactful initiatives and insights.

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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

Education

Master's degree
OR
Doctoral / PhD

Work Experience

5 years

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

Languages

English – Business Fluent

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