Full-Time Associate Director, Toxicology

Nurix Therapeutics is a clinical-stage biopharmaceutical company focused on targeted protein degradation medicines.

Position: Design and management of safety pharmacology, exploratory and GLP toxicology studies. Handle multiple projects.

Responsibilities:

• Lead toxicology strategy and tactics in discovery, preclinical, and clinical development.
• Participate in multi-disciplinary team efforts.
• Serve as the internal study directory and primary point-of-contact with CRO partners.
• Monitor outsourced GLP and non-GLP studies ensuring compliance.
• Write and review toxicology reports.
• Apply toxicology, pharmacology, ADME knowledge, and regulatory guidelines.
• Provide creative approaches to expedite nonclinical development.
• Serve as the Toxicology representative on project teams.
• Contribute to regulatory documents.
• Communicate toxicology study results.
• Travel required.

Required Qualifications:

• Ph.D. in Toxicology, Pharmacology, or related field with 5+ years industry experience.
• Substantial nonclinical development experience.
• Experience in designing, monitoring, and interpreting nonclinical studies.
• Experience in writing and reviewing nonclinical regulatory documents.

Bonus Qualifications:

• Certification by the American Board of Toxicology (DABT).

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