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CSCSL Behring

Director, Nonclinical Due Diligence & External Innovation(m/w/x)

Glattbrugg, Zürich
Vollzeitmit HomeofficeSenior

Leading nonclinical due diligence for biologics and complex modalities, integrating expert input into risk narratives. Advanced degree and 10+ years nonclinical development experience required. Focus on FIH-enabling requirements and clear communication to non-expert stakeholders.

Anforderungen

  • Advanced degree (Ph.D., D.V.M., or equivalent) in toxicology, pharmacology, or related field
  • Toxicology training, board certification preferred
  • 10+ years nonclinical development experience with proven due diligence or external innovation experience across geographies
  • Strong understanding of FIH-enabling nonclinical requirements, particularly for biologics and complex modalities
  • Ability to communicate complex scientific risk clearly to non-expert stakeholders
  • Experience across multiple therapeutic areas and modalities highly desirable
  • Proven ability to work independently or in a team, meeting goals by managing own timelines
  • Experience in cross-functional, multicultural, and international teams
  • Excellent communication and analytical skills
  • Experience analyzing and presenting research results to scientific and professional audiences
  • Strong planning and organizational skills
  • Ability to work successfully in a matrix organizational structure
  • Strong negotiation skills and ability to identify and engage internal and external expertise
  • Good understanding of drug development process, strong knowledge of ICH/GLP

Aufgaben

  • Lead nonclinical due diligence for assigned opportunities
  • Integrate expert input into clear risk narratives
  • Serve as subject-matter lead for nonclinical due diligence on individual deals
  • Execute end-to-end nonclinical due diligence for assets or transactions
  • Combine input from Toxicology, PK/QSP, and Nonclinical Pharmacology into coherent assessments
  • Identify first-in-human gaps, translational risks, and regulatory limitations
  • Propose clear mitigation strategies for identified risks
  • Prepare high-quality due diligence reports, executive summaries, and risk tables
  • Act as scientific interface to Business Development and Therapeutic Area teams
  • Contribute to maintaining and improving nonclinical due diligence frameworks
  • Mentor junior contributors and matrix team members
  • Escalate complex or high-impact issues to Head of Nonclinical Development
  • Chair the NCD Review Committee

Berufserfahrung

  • 10 Jahre

Ausbildung

  • Doktor / Ph.D.

Sprachen

  • Englischfließend
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