Hybrid Associate Director, In Vivo Toxicology

Crispr Therapeutics Inc in; Boston (MA); Hybrid; USD 160,000 - 180,000; Full time

Job summary

CRISPR Therapeutics, Inc. seeks an experienced toxicologist to advance IND-enabling pharmacology studies for in vivo programs.

The role reports to the Director, Head of in vivo Toxicology and acts as a cross-functional SME across toxicology, pharmacology and DMPK to drive nonclinical strategy. Remote work is allowed with a minimum on-site presence; associated duties include collaboration across teams, authoring non-clinical sections for regulatory filings, and supporting early development

Qualifications

• Ph.D. in toxicology or related field with 8+ years of relevant experience.
• Master’s in toxicology or related field with 15+ years of relevant experience is acceptable.

Responsibilities

• Designs non-clinical non-GLP and GLP studies; prepares protocols and supervises studies.
• Supports resourcing for pharmacology, toxicology, and DMPK activities from in vivo studies to IND/LICENSURE.
• Ensures studies meet FDA/CHMP/WHO/GLP/ISO standards and guidelines.

Skills

IND experience

GLP toxicology

DMPK

CRO outsourcing

Regulatory interactions

Education

PhD toxicology

Master's toxicology

Tools

IB/IND documents

Job description

CRISPR Therapeutics, Inc. seeks an experienced toxicologist to advance IND-enabling pharmacology studies for in vivo programs.

The role reports to the Director, Head of in vivo Toxicology and acts as a cross-functional SME across toxicology, pharmacology and DMPK to drive nonclinical strategy. Remote work is allowed with a minimum on-site presence; associated duties include collaboration across teams, authoring non-clinical sections for regulatory filings, and supporting early development