MSD

Medical Affairs Manager


PayCompetitive
LocationNot available
Employment typeFull-Time

What's your preference?

Apply with job updates
  • Job Description

      Req#: R346503

      Job Description

      Medical Affairs Manager

      Overview:
      Under the supervision of the Medical Director, the Medical Affairs Manager (MAM) oversees medical activities for one or more therapeutic areas, collaborating with marketing, market access, policy teams.

      Key Responsibilities:

      • Strategic Contribution: Optimize medical and clinical excellence throughout the product lifecycle to meet business objectives.
      • Medical Affairs Strategy: Develop and implement the Medical Affairs Plan (MAP) for assigned therapeutic areas, managing related budgets.
      • Scientific Interactions: Establish and maintain high-level scientific relationships with healthcare professionals (HCPs), including scientific leaders and societies.
      • Advisory Role: Provide medical and scientific input for business strategies, market access, and health economics.
      • Expert Recognition: Serve as the company’s expert in the therapeutic area among HCPs and colleagues.
      • Regulatory Engagement: Engage with regulatory and reimbursement authorities on scientific and medical matters.

      Strategic Activities:

      • Local Planning: Implement local Medical Affairs activities to enhance the company’s reputation and represent it in cross-functional teams.
      • MAP Development: Create a MAP with strategies aligned to brand imperatives and local healthcare needs.
      • Data Generation: Plan and execute local data generation programs, ensuring compliance with product strategies and securing necessary approvals.
      • Publication Management: Implement publication policies and secure the production of review articles.
      • Event Participation: Identify and engage in relevant meetings, congresses, and CME opportunities.

      External Interactions:

      • Scientific Leadership: Maintain dialogue with scientific leaders and manage national/regional Advisory Boards.
      • CME Contributions: Participate in sponsored meetings and CME events, including speaker engagements and presentations.
      • Guideline Input: Provide input for formulary and clinical guideline development.

      Internal Interactions:

      • Cross-Functional Partnership: Be a valuable partner in cross-functional teams. Act as the medical and scientific expert for therapeutic areas, collaborating with Market Access, Marketing, Policy, Regulatory, and Clinical Operations.
      • Promotional Accuracy: Ensure the scientific accuracy of promotional materials through the review process.

      Skills, Knowledge & Competencies:

      • Proficient understanding of drug development, relevant diseases, and local medical practices.
      • Strong knowledge of therapeutic areas and applicable regulations.
      • Effective collaboration in a matrix organization.
      • Excellent interpersonal and presentation skills.
      • Strong ethical standards and leadership behaviors.
      • Open-mindedness, willingness to learn, and a mindset for sharing ideas.
      • Strategic thinking.
      • Proficiency in English and Czech.

      Education & Experience:

      • Medical Degree (preferred) or PhD/PharmaD in life sciences.

      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:

      Regular

      Relocation:

      No relocation

      VISA Sponsorship:

      No

      Travel Requirements:

      25%

      Flexible Work Arrangements:

      Hybrid

      Shift:

      Not Indicated

      Valid Driving License:

      Yes

      Hazardous Material(s):

      No

      Required Skills:

      Preferred Skills:

      Job Posting End Date:

      05/28/2025

      *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.

  • About the company

      Merck & Co., Inc.

Notice

Talentify is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Talentify provides reasonable accommodations to qualified applicants with disabilities, including disabled veterans. Request assistance at accessibility@talentify.io or 407-000-0000.

Federal law requires every new hire to complete Form I-9 and present proof of identity and U.S. work eligibility.

An Automated Employment Decision Tool (AEDT) will score your job-related skills and responses. Bias-audit & data-use details: www.talentify.io/bias-audit-report. NYC applicants may request an alternative process or accommodation at aedt@talentify.io or 407-000-0000.