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BABayer

Director, Integrated Product Medical Lead(m/w/x)

Basel
Full-timeOn-siteSenior

Leading global oncology drug development programs for early clinical development. M.D. with 5+ years patient care and 3-5 years drug development expertise required. Oncology/hematology board certification a plus.

Requirements

  • M.D. with 5+ years direct patient care
  • Board certification in oncology/hematology or associated subspecialties
  • Track record of relevant research in peer-reviewed publications
  • 3-5 years drug development expertise
  • 2+ years early drug development experience
  • Expertise across different biologies and modalities
  • Expertise in small and large molecules
  • Global health authority interactions
  • Current knowledge of regulatory review and responses
  • Ability to develop sound medical strategy
  • Ability to teach medical strategy development
  • Strong communication skills
  • Strong leadership skills
  • Strategic thinking
  • Good business insights
  • Good external trends insights
  • High energy with focus and vision
  • Self-motivated with high sense of ownership
  • Proactive, solution-oriented approach
  • Mandatory fluency in English
  • Command of a second major European language
  • German language command is an asset

Tasks

  • Lead global development programs in Oncology
  • Set strategic direction for assigned programs
  • Develop end-to-end clinical strategies
  • Execute development programs for Early Clinical Development Oncology (ECDO)
  • Provide clinical-scientific leadership for global programs
  • Collaborate with cross-functional teams to create target product profiles
  • Support internal and external innovation efforts
  • Shape functional excellence within ECDO
  • Drive core project, people, and innovative clinical development topics
  • Act as primary clinical representative for global programs
  • Develop clinical vision for unmet medical needs
  • Ensure timely delivery of milestones
  • Mitigate roadblocks in program execution
  • Support preclinical evaluation of new oncology assets
  • Guide preclinical asset development for informed clinical decisions
  • Review key study documents for alignment with development plans
  • Provide expertise on scientific, development, and regulatory landscapes
  • Interact with academic, industry, and health authority partners
  • Lead strategic initiatives for ECDO, RED-ONC, and Bayer
  • Promote creative collaboration between clinicians and scientists
  • Foster a culture of ownership and peer accountability

Work Experience

  • 5 years

Education

  • Doctoral / PhD

Languages

  • EnglishNative
  • GermanBasic
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