Job Description
Regional Director of Medical Affairs Hematology (MER & EEMEA Region)
The Regional Director of Medical Affairs (RDMA) Hematology for the MER (Mid-Europe Region) and EEMEA (Eastern Europe Middle East and Africa) regions is responsible for driving the planning and execution of scientific & medical affairs plans in the Value & Implementation (V&I) organization for Hematology including Alliances with external partners as applicable. The RDMA is an impactful member of regional cross-functional teams including Global Medical & Scientific Affairs Outcomes Research Commercial Clinical Policy and Market Access. The RDMAs engage with their network of scientific leaders and decision makers in their regions. This is a Europe/EEMEA-based position in Our Companys Research Laboratories V&I Global Medical and Scientific Affairs (GMSA).
Responsibilities and Primary Activities:
Guides country research division Global Medical and Scientific Affairs (GMSA) colleagues to execute the annual scientific & medical affairs plan for their assigned therapeutic areas (TA) in Hematology including Alliances with external partners as applicable.
Chairs the MER/EEMEA Regional Medical Affairs Team (RMAT) to ensure development and execution of agreed medical affairs strategy and tactics to achieve the Value & Implementation (V&I) goals and priorities while providing strategic input at the global level
Ensures scientific exchange is aligned with the global and regional scientific and medical affairs goals and priorities
Consolidates actionable medical insights from countries in their region
Partners with regional Commercial regional Outcomes Research regional Policy and regional Market Access to drive development and execution of regional plans
Engages appropriately with a network of scientific leaders and other key stakeholders (therapeutic guideline committees payers public groups government officials medical societies) from their region about Our Companys emerging science
Supports as regional TA expert affiliates colleagues in engagement with their national scientific leaders
Organizes regional symposia and educational meetings as appropriate
Organizes regional expert input events (advisory boards/group input meetings) to gather insights on Our Companys questions about development/implementation of new medicines
Supports key countries with the development of local data generation (LDG) study concepts and protocols
Reviews investigator-initiated study (IIS) proposals per established process
Manages regional programs (patient support educational or risk management) to support appropriate and safe utilization of our companys medicines
Required Qualifications Skills & Experience:
Minimum
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
Preferred
Hematology role experience (3 years)
Customer expertise especially scientific leadership and other key stakeholders (payers public groups government officials medical professional organizations) in Hematology
Location
The position can be based at any of our offices in Europe or the EEMEA region. Please note that relocation and visa support are not offered.
Required Skills:
Adaptability 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 2 morePreferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
25%Flexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
N/AJob Posting End Date:
01/31/2026*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Required Experience:
Director
Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more