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Merck

Makes medicines, vaccines and animal treatments

Medical Manager - Immunology, Medical Affairs

Biology & BiotechConfirmed live in the last 24 hours
Full-timeNo salary listedIn-person

About the Job

Requirements

  • Clinical trial protocols.
  • Healthcare education.
  • Health technology assessment (HTA).
  • Immunology.
  • Medical affairs.
  • Medical communications.
  • Project management.
  • Scientific leadership.
  • Strategic planning.

Responsibilities

  • Consolidate actionable medical insights to inform company strategies.
  • Translate global medical goals and strategies into tactics and solutions supporting scientific exchange, improved patient outcomes, and enhanced access.
  • Execute tactical plans and adapt them to local business realities.
  • Follow up on Investigator-Initiated Study (IIS) proposals aligned with the company's ISS Program areas of interest.
  • Collaborate with research laboratories and Global Clinical Trial Operations personnel to identify potential investigators for clinical development programs.
  • Facilitate delivery of phase I–IV data-generation activities, including identifying suitable research projects, research centers, investigators, and innovative methods.
  • Provide non-promotional, balanced, and reliable scientific information in accordance with company standards and local regulations.
  • Bring the local scientific and healthcare environment perspective to the Regional Medical Affairs team.
  • Communicate scientific and business needs effectively across internal and external stakeholders.
  • Build trust with the external scientific community through peer-to-peer scientific exchange, research and educational collaborations, and interactions with scientific societies, health organizations, and publications.
  • Provide therapeutic and functional training to assigned teams and affiliate functions.
  • Develop and execute country medical educational programs and symposia.
  • Lead country advisory boards and expert input forums.
  • Participate in and contribute to professional organizations and academic or regulatory working teams.
  • Collaborate on and lead resolution of regulatory, public relations, compliance, and other asset issues.
  • Support resolution of asset safety or quality issues, including contributing content and strategy for regulatory responses and interactions, risk management planning, and implementation.
  • Provide access support as needed, including health technology assessment, pre-license patient access, and reimbursement dossiers.

About the Company

Merck

Makes medicines, vaccines and animal treatments

Merck develops prescription medicines, vaccines and veterinary treatments for patients, health systems and animal owners worldwide. Its vaccine portfolio includes Gardasil 9, which helps prevent cancers and other diseases caused by several types of human papillomavirus. The company takes potential treatments through laboratory research and clinical trials, then manufactures and sells approved products to drug distributors, hospitals, physicians and governments. Its animal health division sells medicines and vaccines to veterinarians, farmers and pet owners, while selected drug partnerships also earn shared profits or royalties. Founded in 1891, Merck is headquartered in Rahway, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Rahway, NJ
Founded
1891

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