Medical Affairs Specialist (temporary)

Merck Merck · Pharma · Cundinamarca, Colombia

This role supports Medical Operations within the Global Medical Affairs Capabilities Hub at Merck, focusing on communication, meeting organization, and execution of Medical Operations initiatives. It involves supporting tools like X-Fly insights, managing the Country-to-Country (C2C) program, creating reports, and collaborating with global and country-level teams. The position requires a Bachelor's degree, 5+ years of Medical Affairs experience, strong English proficiency, and expertise in Microsoft Office Suite. Key responsibilities include supporting strategic initiatives, ensuring compliance with SOPs and regulations, and acting as a subject matter expert in V&I systems. The role demands strong organizational, problem-solving, and analytical skills, with an emphasis on adaptability and detail orientation within a complex, regulated environment.

What you'd actually do

  1. Ensures MO support to further develop and maintain a highly functioning V&I organization.
  2. Supports and advises on X-Fly insights tool for users and quarterly report for tracking regional and countries backlogs.
  3. Supports the Country-to-Country (C2C) program, process overview and report on number of C2C requests sent/received, economic inversion, and special cases.
  4. Creates and shares reports for the main stakeholders (Process and Systems).
  5. Collaborates and support Global V&I Operations and Country Medical Operations (CMO) teams

Skills

Required

  • Bachelor’s degree in life sciences, business or health care.
  • 5+ years of relevant Medical Affairs experience (e.g., Strategic Support, V&I Operations).
  • Advance English
  • Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint) and MS Office 365 (Teams, SharePoint, etc.)
  • Track record as a deadline-oriented self-starter with frequent outreach to teams to maintain project timelines.
  • Understanding of the environment, evolution and global nature of Medical Affairs.
  • Demonstrated experience in identifying process gaps and building new processes.
  • Experience as a member in cross-functional initiatives in a complex matrix.
  • Experience working within regulations and compliance requirements.
  • A thorough understanding of ethical guidelines relevant to the pharmaceutical industry to ensure compliance with external and internal guidelines and standard operating procedures.
  • Adaptability
  • Business Strategies
  • Clinical Medicine
  • Data Analysis
  • Detail-Oriented
  • Global Health
  • Healthcare Education
  • Life Science
  • Medical Affairs
  • Medical Communications
  • Medical Knowledge
  • Medical Review
  • Medical Writing
  • Microsoft Office
  • Microsoft Online Services
  • Microsoft Teams
  • Pharmaceutical Management
  • Pharmaceutical Medical Affairs
  • Professional Integrity
  • Project Management
  • Promotional Review
  • Scientific Literature
  • Standard Operating Procedure (SOP)
  • Strategic Initiative

What the JD emphasized

  • experience working within regulations and compliance requirements
  • A thorough understanding of ethical guidelines relevant to the pharmaceutical industry to ensure compliance with external and internal guidelines and standard operating procedures.