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Study Director Toxicology Jobs (NOW HIRING)

Frontage Laboratories

Director of Toxicology

Chicago, IL · On-site

$150K - $200K/yr

This leadership role will be responsible for overseeing study design, execution, and interpretation of nonclinical toxicology studies, while managing and mentoring a team of Study Directors and ...

RPM ReSearch

$125K - $130K/yr

Principal Scientist / Study Director (Toxicology) Build Programs. Lead Science. Influence Outcomes. Why This Role Matters Here, toxicology isn't just about executing studies--it's about shaping how ...

Evommune, Inc.

Director, Toxicology

Palo Alto, CA · On-site

The Director will serve as the toxicology representative on cross-functional program teams and will ... Ensure studies are conducted in accordance with GLP requirements, applicable regulations, and ...

Inotivco

Director, Toxicology

Gaithersburg, MD

$120.20 - $175K/hr

Approves interpretation of study data and final reports prepared by other study directors ... General Toxicology. * Recognizes potential training needs in preparation for new business ...

RPM ReSearch

Study Director

West Sacramento, CA

$74K - $110K/yr

Join Our Team as a Study Director and Research Scientist! Your New Opportunity: We're all about ... Experience in Toxicology is a plus. * Skills: Intermediate to Advanced Computer Skills, strong ...

Inotiv

Director, Toxicology

Gaithersburg, MD · On-site

$120.20 - $175K/hr

Approves interpretation of study data and final reports prepared by other study directors ... General Toxicology. * Recognizes potential training needs in preparation for new business ...

Certara USA, Inc.

Director, Toxicology

Wayne, PA · On-site

Our Toxicology Directors support projects for Certara's clients by working in teams with other ... Outline studies and in partnership with clients, identify CROs to run these studies; manage the ...

Tarsus Pharmaceuticals

Director, Toxicology

Irvine, CA · On-site +1

About the Role The Director, Toxicology Translational Science will serve as a scientific and ... Review and edit study protocols and reports to ensure scientific rigor, regulatory compliance (GLP ...

Tarsus Pharmaceuticals

Director, Toxicology

Irvine, CA · On-site

About the Role The Director, Toxicology Translational Science will serve as a scientific and ... Review and edit study protocols and reports to ensure scientific rigor, regulatory compliance (GLP ...

OnKure Therapeutics

Senior Director, Toxicology

Boulder, CO · On-site

$280K - $300K/yr

The Senior Director of Toxicology provides strategic and scientific leadership for all nonclinical ... Safety pharmacology studies * IND-enabling and post-IND toxicology studies, including genotoxicity ...

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Study Director Toxicology information

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$45K

$128.4K

$232.5K

How much do study director toxicology jobs pay per year?

As of Jul 26, 2026, the average yearly pay for study director toxicology in the United States is $128,367.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $188,500.00 per year, depending on experience, location, and employer.

What does a Study Director in Toxicology do?

A Study Director in Toxicology is responsible for overseeing and managing toxicology studies that assess the safety of chemicals, pharmaceuticals, or other substances. They design study protocols, ensure compliance with regulatory guidelines, supervise laboratory staff, and interpret study data. Study Directors are the single point of control for each study, ensuring that studies meet scientific and regulatory standards and that accurate, reliable data are reported to clients or regulatory agencies.

What is the difference between Study Director Toxicology vs Toxicology Associate?

AspectStudy Director ToxicologyToxicology Associate
Required CredentialsBachelor's or Master's in Toxicology, Pharmacology, or related field; often requires experience in GLP studiesTypically Bachelor's degree in Toxicology, Biology, or related field; entry-level role
Work EnvironmentLead study planning, oversee testing, ensure compliance in GLP labsAssist with sample preparation, data collection, and lab support tasks
Employer & Industry UsagePharmaceutical, biotech, contract research organizations (CROs)Similar industries, often as entry-level or support staff

The Study Director Toxicology is a senior role responsible for overseeing toxicology studies and ensuring regulatory compliance, while a Toxicology Associate provides support in laboratory tasks. The Study Director typically has more experience and credentials, focusing on study management, whereas the Associate assists with data collection and sample handling.

What are the key skills and qualifications needed to thrive as a Study Director in Toxicology, and why are they important?

To thrive as a Study Director in Toxicology, you need a robust background in toxicology or related life sciences, often supported by an advanced degree (e.g., PhD or MSc) and experience in GLP-compliant research. Familiarity with laboratory information management systems (LIMS), toxicological assay methods, and regulatory guidelines such as OECD and FDA is essential. Strong organizational skills, leadership, and effective communication help in managing multidisciplinary teams and client relationships. These skills ensure the integrity, compliance, and successful delivery of toxicology studies that support regulatory submissions and product safety.

How does a Study Director in Toxicology typically collaborate with cross-functional teams during a study?

A Study Director in Toxicology often works closely with scientists, laboratory technicians, quality assurance personnel, and regulatory affairs teams throughout a study. They coordinate study design, ensure protocols are followed, and address any technical issues that arise. Regular meetings and clear documentation help facilitate communication and keep the study on track. This collaborative environment ensures that all regulatory requirements are met and that data integrity is maintained from start to finish.
More about Study Director Toxicology jobs
What cities are hiring for Study Director Toxicology jobs? Cities with the most Study Director Toxicology job openings:
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Study Director Toxicology jobs near you
Infographic showing various Study Director Toxicology job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $128,367 per year, or $61.7 per hour.
Scientist/ Study Director Toxicology - Preclinical CRO

Scientist/ Study Director Toxicology - Preclinical CRO

RPM ReSearch

Columbia, MO • On-site

Full-time

Posted 17 days ago

Job description

Senior Study Director/ Toxicologist


We are a growing mid-size organization with multiple sites looking for an accomplished Senior Study Director for our Toxicology division to assist with the growth we are experiencing and have plans to continue.


Say Goodbye to the bureaucracy and the administrative aspects of large cumbersome organizations and say Hello to the Science!


As a Senior Study Director, you will be responsible for participating in the design of non-clinical / preclinical studies as well as providing the scientific oversight of the study.

These studies will involve standard laboratory animal species (mice, rats, NHP, swine) across typical test article types (Vaccines, Biopharmaceuticals, Small Molecules).

This role will encompass multiple site studies and coordination thereof.


  • Maintaining and completing multiple projects simultaneously

  • Developing Protocols

  • Communicating with staff, management, and clients/sponsors

  • Analysis, interpretation, and reporting of data from non-clinical studies.

  • Manage the conduct of study activities in compliance with the protocol, amendments, and facility SOPs

  • May also assist in the further development of SOPs, training materials, and policies.

  • Proactive recognition, documentation, and resolution of any issues affecting the conduct of non-clinical studies.

  • Maintain knowledge of FDA and other regulatory guidelines

  • Work with the appropriate individuals to design and approve the study protocols

  • Perform other duties directed by the Director of Toxicology to meet client needs.


Experience, Education, and Specialized Knowledge and Skills:

Education

At least 5 years of experience directing non-clinical in vivo studies at a CRO or Pharmaceutical Company with a BS

-or-

At least 2 years of relevant industry/ toxicology experience with an MS or Ph.D./DVM

DABT or board eligible preferred

Demonstrated expertise in a scientific discipline


Essential Skills include: leadership, good organizational skills, knowledge of an experience with GLP (Good Laboratory Practices), AAALAC and USDA guidelines, experience using computer applications.