Associate Director - Toxicology

February 20

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Logo of Nurix Therapeutics

Nurix Therapeutics

Nurix Therapeutics is a biotechnology company that is leading the field of protein modulation to develop innovative medicines for cancer and inflammatory diseases. The company leverages its proprietary DELigase platform to create small molecule drugs that harness the activity of E3 ligases, enzymes crucial for protein degradation within cells. Nurix's approach involves both targeted protein degradation, which eliminates specific disease-causing proteins, and targeted protein elevation, which prevents protein degradation to raise levels of beneficial proteins. Through its advanced pipeline, Nurix aims to meet the unmet medical needs of patients by empowering the body's natural ability to fight disease.

research β€’ life sciences β€’ biotechnology

201 - 500 employees

Founded 2015

🧬 Biotechnology

πŸ’Š Pharmaceuticals

πŸ”¬ Science

πŸ’° $40M Post-IPO Equity on 2022-07

πŸ“‹ Description

β€’ Design and management of safety pharmacology, exploratory and GLP toxicology studies. β€’ Lead toxicology strategy and tactics in discovery, preclinical development and clinical development. β€’ Serve as the internal study directory and primary point-of-contact with CRO partners. β€’ Write and review toxicology reports and documentation for regulatory filings. β€’ Provide creative approaches to expedite nonclinical development strategies. β€’ Effectively communicate toxicology study results to project teams and senior level management. β€’ Travel required as needed.

🎯 Requirements

β€’ Ph.D. in Toxicology, Pharmacology, or a related field with a minimum of 5 years of industry experience as part of a drug development project team or a minimum of 5 years FDA experience reviewing nonclinical regulatory submissions. β€’ Substantial nonclinical development experience at a pharmaceutical or biotechnology company or with the FDA. β€’ Experience in designing, monitoring and interpreting nonclinical toxicology/safety pharmacology studies. β€’ Experience in writing and reviewing nonclinical sections of regulatory documents (CTA, IND, IB, NDA, BLA, etc.) and direct interactions with worldwide regulatory agencies. β€’ Certification by the American Board of Toxicology (DABT) is highly desired.

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πŸ‡ΊπŸ‡Έ United States – Remote

πŸ’΅ $206.2k - $270.7k / year

πŸ’° Post-IPO Equity on 2023-11

⏰ Full Time

🟠 Senior

πŸ‘” Director

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