Regional Director, Medical Affairs, HIV, EEMEA
Job Description The Regional Director Medical Affairs (RDMA) is responsible for driving execution of scientific & medical affairs plans for HIV Therapy Area (TA) in the countries of their assigned region. They are impactful members of regional cross-functional teams, including regional Commercial, Outcomes Research (OR), Market Access, and Policy. They engage with their network of scientific leaders in their region.
This is a regionally based position (i.e. residing in one of the affiliates of the region or regional hub) in Our Company Research Laboratories Global Medical and Scientific Affairs (Research & Development GMSA) team. The EEMEA region includes Eastern Europe, Middle East, and Africa.
Responsibilities and Primary Activities:
- Guides country R&D GMSA staff on strategic planning and execution of the annual scientific & medical plan for HIV Therapy Area
- Chair or participate in the Regional Value and Implementation Team (RVIT) to ensure strategic alignment and execution of agreed medical tactics within the region, including the development of cross-functional regional V&I goals
- Partners with regional Commercial, regional Center of Real-World Evidence (CORE), regional Policy and regional Market Access to drive development and execution of region plans
- Support development of global V&I plans based on regional input related to insights, unmet needs, and priority evidence data gaps
- Ensures scientific exchange is aligned with the global scientific communications platform
- Consolidates actionable medical insights from countries in their region
- Engages with a network of contracted Scientific Leaders (SL) and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) from their region
- Supports, as regional TA expert, affiliates staff in engagement with their national scientific leaders
- Organizes regional expert input events to answer Our Company’s questions regarding how to implement new indications: advisory boards and expert input forums
- Organizes regional symposia and educational meetings
- Supports countries with the development of local data generation study concepts and protocols
- Reviews investigator-initiated study (IIS) proposals prior to headquarters submission (ex-USA) and participate in IIS review committee as presenter and concept reviewer
- Manages regional programs (patient support, educational or risk management) to support appropriate and safe utilization of Our Company’s medicines
- Support planning and execution of scientific coverage efforts for major international conferences
Minimum:
- MD, PhD or PharmD (MD preferred) and recognized medical expertise in the therapy area
- Five+ years’ experience in country / region Medical Affairs
- Strong prioritization and decision-making skills
- Able to effectively collaborate with partners across divisions in a matrix environment
- Excellent interpersonal, analytical, communication (written as well as oral) skills, in addition to results-oriented project management skills
- HIV and ID experience
- Experience as scientific leader and other key stakeholders (payers, public groups, government officials, medical professional organizations) in the assigned therapeutic area
- The position can be based at any of our offices in Europe or the EEMEA region.
Preferred Skills:
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Employee Status:
Regular
Relocation:
No relocation
VISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
Remote
Shift:
Not Indicated
Valid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
08/2/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.