3 часа назад
Director, Nonclinical Due Diligence & External Innovation
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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