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Director, Nonclinical Due Diligence – External Innovation
CSLDirector leading scientific evaluations for nonclinical due diligence in global biotherapeutics. Supporting CSL’s in‑licensing, acquisitions, and strategic collaborations.
About the role
Key responsibilities & impact- Provides scientific leadership for nonclinical due diligence supporting CSL’s in‑licensing, acquisitions, and strategic collaborations.
- Leads operational execution of nonclinical due diligence for assigned opportunities.
- Acts as hands‑on scientific integrator, translating expert input into clear risk narratives.
- Integrates input from Toxicology, PK/QSP, Nonclinical Pharmacology, and external experts.
- Prepares high‑quality DD reports, executive summaries, and risk tables for governance review.
- Mentors junior contributors and matrix team members as appropriate.
Requirements
What you’ll need- Advanced degree (Ph.D., D.V.M., or equivalent) in toxicology, pharmacology, or a related field
- 10+ years of experience in nonclinical development
- Strong understanding of FIH-enabling nonclinical requirements
- Excellent communication skills
- Strong planning and organizational skills
- Fluent in English, oral and written
Benefits
Comp & perks- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
toxicologypharmacologynonclinical developmentrisk assessmentdue diligencereport writingdata analysisstrategic collaborationexpert integrationFIH-enabling requirements
Soft Skills
scientific leadershipmentoringcommunicationplanningorganizational skills
Certifications
Ph.D.D.V.M.