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Global Director Medical Affairs

Il y a 2 mois

Paris, Île-de-France MSD France Temps plein
Job Summary

We are seeking a highly skilled and experienced Global Director Medical Affairs to join our team at MSD France. The successful candidate will be responsible for coordinating the development and implementation of Global Medical Affairs Plans for Oncology Pipeline Assets.

Key Responsibilities
  • Asset Management & Business Leadership
    • Develop and implement medical goals and strategies that inform and demonstrate scientific & clinical value and address insights from affiliates and regions.
    • Translate these goals and strategies into research, data analysis, scientific communication, educational, and other tactics and solutions that improve patient outcomes and enhance access.
    • Contribute substantively to and be a valued co-strategist on asset cross-functional meetings: Franchise Teams, Clinical, Outcomes Research, Risk Management, and Commercial Asset Development Subteams, Publication Teams, Rapid Response Teams.
    • Inform Life Cycle Management decisions leveraging patient and healthcare country insights.
    • Support business development assessments by validating unmet medical needs, reviewing asset data (through a medical affairs lens), and recommending required medical affairs resources.
    • Support integrated data generation plans and co-develop clinical and outcomes research programs with cross-functional R&D and Observational Research colleagues that address life cycle management needs.
    • Advise on areas of interest for the Investigator-Initiated Study Program.
    • Execute on and quickly adapt portfolio of tactics to life-cycle stage and business realities.
    • Lead medical affairs coordination in alliances that our company may have with other pharmaceutical companies.
  • Scientific & Technical Leadership
    • Communicate both scientific and business needs credibly and effectively across a variety of internal and external stakeholders at all levels, including external scientific leaders and key decision makers.
    • Develop/support initiatives to improve internal education about the pipeline agents and specific projects under the Innovative Strategy group.
    • Contributions at MISP and sponsored Protocol Review Committees (PRCs).
    • Build trust with the external scientific community via peer-to-peer interactions, research and educational collaborations, interactions with global scientific societies and health organizations, publications, or other relevant stakeholders.
    • Develop and execute global Group Input Meetings (advisory board meetings) in partnership with Executive Directors of Scientific Affairs to inform life cycle management decisions.
    • Develop and execute global symposia and educational meetings. Work with Regional Directors Medical Affairs for regional symposia and meetings.
    • Participate in and contribute significantly to professional organizations, academic or regulatory working teams.
    • Successfully collaborate and lead resolution of regulatory, reputational (i.e. public relations), compliance and other asset issues management.
    • Substantive contributions to labeling committees. Ensure labels contain fair-balanced claims supported by data and supportive of asset-related medical, clinical and scientific value requirements for most geographies.
  • Management
    • Participate during relevant Global Medical Affairs Team (GMAT) related to assigned to asset(s). Collaborate with the relevant TA teams, either at global and regional level for the execution of the relevant medical plans associated with pipeline compounds and Innovative Strategies projects.