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BOBoehringer Ingelheim

Medical Affairs Lead Obesity Triple Agonist(m/w/x)

Ingelheim am Rhein
Full-timeOn-siteSenior

Shaping global Medical Affairs strategy for obesity triple agonist, leading scientific and clinical excellence. M.D. or Ph.D. with extensive obesity/GLP-1 Medical Affairs leadership experience required. Comprehensive benefits package, wellbeing package.

Requirements

  • M.D. or Ph.D. with extensive Medical Affairs leadership experience in obesity and/or GLP-1 segment
  • Strong foundational knowledge of clinical drug development
  • Senior leadership experience in global, regional, and/or key-market Medical Affairs roles
  • Accountability for strategy, governance, and people leadership
  • Develop externally focused, competitive Medical Affairs strategies
  • Experience supporting label shaping, regulatory interactions, and pre-launch evidence readiness
  • Support late-stage development, launch preparation, and post-launch medical excellence
  • Interactions with Health Authorities in major markets (US, EU)
  • Cross-functional leadership and influence in complex global matrix environments
  • Excellent communication, presentation, and influencing skills
  • Credibility at senior internal and external scientific levels
  • Build, lead, and develop high-performing Medical Affairs teams
  • Persons with severe disabilities warmly welcomed
  • Preferential consideration for equally qualified disabled applicants

Tasks

  • Shape global Medical Affairs strategy for obesity triple agonist
  • Lead scientific, clinical, and medical excellence across asset lifecycle
  • Translate science into value through evidence generation and communication
  • Provide strategic input into overarching asset decisions
  • Partner with Global Development, Market Access, and Commercial functions
  • Build and lead a high-performing global Medical Affairs organization
  • Ensure external credibility and impactful scientific engagement
  • Represent Medical Affairs on Global Brand Leadership Team
  • Contribute to governance and strategic decision-making
  • Provide medical leadership for Phase III development
  • Develop indication strategy and lifecycle planning
  • Drive Integrated Evidence Plan with Clinical Development and Market Access
  • Engage with Health Authorities, HTA bodies, and key stakeholders
  • Support future labeling, access, and adoption
  • Partner with regional and local Medical Affairs teams
  • Ensure launch readiness and post-launch excellence globally
  • Integrate clinical and real-world evidence into medical narratives
  • Develop scalable capabilities and top talent

Work Experience

  • approx. 4 - 6 years

Education

  • Doctoral / PhD

Languages

  • EnglishBusiness Fluent

Benefits

Other Benefits

  • Comprehensive benefits package

Mental Health Support

  • Wellbeing package
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