MU
Mundipharma Holding AG
22 Tage

Medical Affairs Cluster Lead LCM(m/w/x)

Vollzeit
Senior
Keine Angabe
Basel

In this role, you will lead Medical Affairs for the LCM cluster, focusing on enhancing patient outcomes through innovative medical plans and strong collaborations. Your daily responsibilities will include coaching teams, managing budgets, and ensuring compliance while driving impactful medical evidence generation.

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Anforderungen

  • MD or equivalent
  • 12+ years in Medical Affairs, including 3–5 years as Country Medical Director
  • 3+ years in Clinical Practice
  • Clinical and/or Industry experience in Anti-Infectives
  • Fluency in English (written and spoken)
  • Knowledge in analgesic and pain therapeutic areas
  • Good knowledge of compliance in Medical Affairs
  • Extensive experience leading Medical Affairs teams across markets
  • Successful launch experience in Specialty Care and/or Rare Disease
  • Track record of building scientific partnerships with Key External Experts
  • Extensive experience leading Field Medical teams
  • Deep expertise in setting and monitoring objectives, KPIs, and metrics
  • Track record of excellence in cross-functional working
  • Clinical Development/Operations experience
Master-Abschluss

Berufserfahrung

12 Jahre

Deine Aufgaben

  • Lead Medical Affairs across the LCM cluster
  • Focus on improving patient outcomes
  • Develop and execute Anti-Infective and Subsitol Medical Plans
  • Coach and support Country Medical Advisors
  • Ensure medical governance and compliance with laws and regulations
  • Partner with Global Medical Anti-Infective and Subsitol team
  • Collaborate with Global Pain and Established Brands teams
  • Manage Cluster Medical budgets
  • Work with Global Medical Operations on systems and processes
  • Build a Specialty Care culture centered on patient centricity
  • Contribute to the worldwide Medical Affairs strategy
  • Establish scientific collaborations with external experts and institutions
  • Oversee patient engagement activities with advocacy groups
  • Support local CMDs in resolving disputes with competitors
  • Provide medical expertise to cross-functional teams
  • Advise on scientific and medical matters in Anti-Infectives
  • Partner with Cluster GMs for initiative execution
  • Liaise with Regulatory Affairs, Drug Safety, and R&D
  • Oversee development and approval of promotional materials
  • Collaborate with legal and compliance teams for standards adherence

Sprachen

Englischverhandlungssicher

Deine Vorteile

Weiterbildungsangebote

  • Opportunities for learning & development

Lockere Unternehmenskultur

  • Collaborative work environment
  • Inclusive work environment
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Mundipharma Holding AG erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.

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