The Director Non‑Clinical Due Diligence & External Evaluations provides scientific leadership for nonclinical due diligence supporting CSL’s in‑licensing, acquisitions, and strategic collaborations. The role ensures integrated, objective, and decision‑relevant evaluations of nonclinical pharmacology, PK/QSP, and toxicology data to identify development risks, data gaps, and mitigation strategies and to inform portfolio decisions. The incumbent will further act as nonclinical representative for selected Research programs and support oversight of nonclinical strategies and programs across all Therapeutic Areas. The role reports to the Executive Director, Head of Nonclinical Development.

Responsibilities and Accountabilities

• Lead operational execution of nonclinical due diligence for assigned opportunities.
• Act as hands‑on scientific integrator, translating expert input into clear risk narratives.
• Trusted subject‑matter lead for nonclinical DD o...