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3 часа назад

Director, Nonclinical Due Diligence & External Innovation

Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
c1
Страна
US/Australia/Switzerland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Director, Nonclinical Due Diligence & External Innovation (Nonclinical Development): Leading integrated scientific evaluations of nonclinical pharmacology, PK/QSP, and toxicology data for in-licensing, acquisitions, and strategic collaborations with an accent on identifying development risks, data gaps, and mitigation strategies. Focus on translating cross-functional expert input into governance-ready risk narratives, assessing FIH-enabling requirements, and supporting nonclinical strategy across therapeutic areas.

Location: Zurich, Switzerland or Waltham, USA; onsite presence required 3 days per week

Company

hirify.global is a global biotherapeutics company developing and delivering therapies for rare and serious diseases, including immunology, hematology, cardiovascular, metabolic, respiratory, and transplant conditions.

What you will do

  • Lead end-to-end nonclinical due diligence for individual assets and transactions, from initial request through governance readout.
  • Integrate toxicology, PK/QSP, nonclinical pharmacology, and external expert input into coherent scientific assessments.
  • Identify FIH-enabling gaps, translational risks, regulatory limitations, and appropriate mitigation strategies.
  • Prepare due diligence reports, executive summaries, and risk tables for governance review.
  • Serve as the nonclinical scientific interface for Business Development and Therapeutic Area teams.
  • Improve nonclinical due diligence frameworks and templates, while mentoring junior and matrix team members.

Requirements

  • Advanced degree such as a Ph.D., D.V.M., or equivalent in toxicology, pharmacology, or a related field.
  • At least 10 years of experience in nonclinical development, including due diligence or external innovation.
  • Strong understanding of FIH-enabling nonclinical requirements, particularly for biologics and complex modalities.
  • Knowledge of the drug development process and strong knowledge of ICH and GLP.
  • Experience working in cross-functional, multicultural, international, and matrix environments.
  • Fluent English, both written and spoken, is required.

Nice to have

  • Toxicology training or board certification.
  • Experience across multiple therapeutic areas and modalities.

Culture & Benefits

  • Work within a global biotherapeutics organization serving patients in more than 100 countries.
  • Collaborate with international and multicultural teams across research and therapeutic areas.
  • Contribute to innovation across plasma fractionation, recombinant protein technology, and cell and gene therapy platforms.
  • Access CSL employee benefits and an inclusion-focused workplace.

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