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Toxicology Cro Jobs (NOW HIRING)

Immunome, Inc.

Director, Toxicology

Bothell, WA · On-site

Manage CRO performance, timelines, budgets, and scientific deliverables. Cross-Functional Leadership * Represent Toxicology on cross-functional project teams. * Partner with Clinical Pharmacology ...

Legend Biotech USA, Inc.

$92K - $126K/yr

Working knowledge of GLP toxicology studies, nonclinical pharmacology studies, CRO management, and regulatory expectations for nonclinical development.Experience contributing to IND/CTA-enabling ...

Legend Biotech US

Sr. Scientist, Toxicology

Philadelphia, PA · On-site

$92K - $126K/yr

Working knowledge of GLP toxicology studies, nonclinical pharmacology studies, CRO management, and regulatory expectations for nonclinical development. * Experience contributing to IND/CTA-enabling ...

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How much do toxicology cro jobs pay per year?

As of Aug 7, 2026, the average yearly pay for toxicology cro in the United States is $115,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,000.00 and $135,500.00 per year, depending on experience, location, and employer.
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Toxicology Cro jobs near you
Infographic showing various Toxicology Cro job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 70% Physical, 3% Hybrid, and 27% Remote job distribution, with an average salary of $115,369 per year, or $55.5 per hour.

Associate Director, Toxicology

Latigo Bio

San Francisco, CA • On-site

Full-time

Re-posted 21 days ago

Job description

Salary: $200,000 - $230,000

We are seeking a highly motivated and experienced Associate Director of Toxicology (Nonclinical Safety) to support the advancement of our pipeline programs. This individual will play a key role in designing, executing, and interpreting nonclinical safety strategies across discovery and development programs. This role will contribute to research and development programs.

The successful candidate will serve as a subject matter expert on cross-functional teams and contribute to regulatory strategy, ensuring that nonclinical programs are scientifically robust and aligned with development timelines.


Key Responsibilities:

Nonclinical Strategy & Leadership

  • Serve as the nonclinical safety/toxicology subject matter expert on multidisciplinary project teams
  • Provide integrated assessments of nonclinical data and evaluate overall risk/benefit profiles
  • Contribute to development candidate selection and overall program strategy

Study Design & Execution

  • Design, oversee, and monitor nonclinical safety studies, including:
    • Exploratory/non-GLP toxicology studies
    • IND-enabling toxicology and safety pharmacology studies
    • Post-IND studies (e.g., sub-chronic, chronic, reproductive, carcinogenicity)
  • Manage and oversee CROs and external vendors, including study design, execution, and data quality

Data Analysis & Interpretation

  • Analyze and interpret nonclinical study data to support program decisions
  • Prepare and present findings, and provide guidance to internal stakeholders and governance teams
  • Identify data gaps and proactively develop mitigation strategies

Regulatory Support

  • Author and review nonclinical sections of regulatory documents, including:
    • INDs
    • Investigators Brochures (IBs)
    • Briefing books and responses to health authorities
  • Partner with Regulatory Affairs to support interactions with agencies (e.g., FDA)
  • Ensure compliance with GLP, ICH, and applicable regulatory guidelines

Cross-Functional Collaboration

  • Work closely with Discovery, DMPK, Clinical Pharmacology, Clinical Development, and Regulatory teams
  • Contribute to integrated development plans and timelines
  • Support portfolio-level decision-making through scientific insight


Qualifications

Education & Experience

  • PhD in Toxicology, Pharmacology, or related scientific discipline
  • DABT board certification is preferred
  • ~10+ years of industry experience in nonclinical safety/toxicology
  • Experience supporting small molecule drug development programs preferred
  • Experience with IND-enabling and regulatory toxicology strategies required

Core Competencies

  • Strong scientific judgment and problem-solving capabilities
  • Excellent communication and presentation skills
  • Ability to work effectively in cross-functional, fast-paced environments
  • Collaborative, proactive, and detail-oriented mindset

Technical Skills

  • Strong knowledge of GLP regulations, ICH guidance, and regulatory expectations
  • Experience designing, monitoring, and interpreting nonclinical safety studies
  • Familiarity with CRO oversight and external vendor management


Preferred Qualifications

  • Experience supporting regulatory submissions and agency interactions
  • Background in pain, neuroscience, or related therapeutic areas
  • Prior experience in early-stage biotech environments