About The Position

Role Summary: The Sr. Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans for Dermatology in key countries and regions. They are impactful members of Product Development Team sub-teams and Global Human Health commercialization teams. They collaborate with our Research & Development Division's Early and Late Development functional areas, Value & Implementation Outcomes Research (VIOR), Policy, Commercial and Market Access to address opportunities in key countries. They engage with their network of scientific leaders and decision makers. This is a headquarters-based position in Our Company Research Laboratories Value & Implementation Global Medical and Scientific Affairs (Research & Development (R&D) VI GMSA).

Requirements

  • M.D., Ph.D. or Pharm.D. (M.D. preferred) and recognized medical expertise in Dermatology.
  • Minimum of 3 years of experience in global/region medical affairs or clinical development.
  • 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.

Nice To Haves

  • At least 5 years Global medical affairs experience with proven track record of contribution to medical affairs strategies.
  • Customer expertise, especially of scientific leadership and other key stakeholders (payers, public groups, government officials, medical professional organizations) in the assigned therapeutic area.

Responsibilities

  • Supports execution of the annual Value & Implementation plan with medical affairs colleagues from key countries and regions.
  • Serves as an impactful member of Product Development Team sub-teams (e.g., Clinical, V & I, Commercial, Publications).
  • Contributes to the development of a single global scientific communications platform.
  • Consolidates actionable medical insights from countries and regions.
  • Engages with a network of international scientific leaders and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) about Our Company’s emerging science.
  • Organizes global expert input events (advisory boards and expert input forums) to answer Our Company’s questions about how to develop and implement new medicines or vaccines.
  • Aligns plans and activities with Global Human Health (commercial) executive directors.
  • Organizes global symposia and educational meetings.
  • Supports key countries with the development of local data generation study concepts and protocols.
  • Reviews Investigator-Initiated Study proposals from key countries prior to headquarters submission (ex-USA).
  • Manages programs (patient support, educational or risk management) to support appropriate and safe utilization of Our Company medicines or vaccines.

Benefits

  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
  • We offer a comprehensive package of benefits.
  • Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.
  • More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits .

Stand Out From the Crowd

Upload your resume and get instant feedback on how well it matches this job.

Upload and Match Resume

What This Job Offers

Job Type

Full-time

Career Level

Director

Education Level

Ph.D. or professional degree

Number of Employees

5,001-10,000 employees

© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service