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Study Director Toxicology Jobs (NOW HIRING)

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 ...

RPM ReSearch

Study Director II

Corpus Christi, TX · On-site

$80K - $110K/yr

Study Director - Non-Human Primate Research Program Location: Corpus Christi, Texas Job Type ... toxicology. * Experience managing NHP studies is highly preferred. * Strong communication and ...

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 ...

Vir Biotechnology

Director, Toxicology

San Francisco, CA · On-site

$203K - $284K/yr

THE OPPORTUNITY Vir Biotechnology is seeking an experienced Director, Toxicology to lead non ... You will contribute to study design, data interpretation, regulatory submissions (IND and NDA/BLA ...

Ionis

Associate Director, Toxicology

Carlsbad, CA · On-site

Manage outsourced toxicology studies at CROs, including study design, protocol and report review ... direct authority across scientific and functional teams * Proven ability to convey advanced ...

Calibr

SENIOR DIRECTOR, TOXICOLOGY

San Diego, CA

The Senior Director of Toxicology will be the primary toxicology expert across our pipeline ... Design, oversee, and interpret toxicology studies across a range of modalities, including in vitro ...

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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 Aug 8, 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 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 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 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:
What states have the most Study Director Toxicology jobs? States with the most job openings for Study Director Toxicology jobs include:
What job categories do people searching Study Director Toxicology jobs look for? The top searched job categories for Study Director Toxicology jobs are:
Study Director Toxicology jobs near you
Infographic showing various Study Director Toxicology job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $128,367 per year, or $61.7 per hour.

Director, Toxicology

Tarsus Pharmaceuticals

Irvine, CA • On-site

Full-time

Medical, Dental, Vision, PTO

Re-posted 12 days ago

Job description

About the Role
The Director, Toxicology Translational Science will serve as a scientific and strategic leader driving team and pipeline development at Tarsus, leveraging expertise in toxicology, safety pharmacology, and translational science to bridge discovery and clinical development from concept through IND-enabling and early clinical studies.
Let's talk about some of the key responsibilities of the role:
  • Subject Matter Expert in toxicology, safety pharmacology and nonclinical safety assessment across all Tarsus Programs
  • Establish and maintain strong external partnerships with CROs, academic institutions and key opinion leaders
  • Define and drive GLP- safety /toxicology strategies across programs to accelerate programs to FIH
  • Oversee GLP and non-GLP toxicology and safety pharmacology studies at CROs, ensure scientific rigor, data integrity, and regulatory compliance (GLP, animal welfare, and safety), SOPs, and technical study requirements
  • Review and edit study protocols and reports to ensure scientific rigor, regulatory compliance (GLP, animal welfare, and safety), and high-quality study interpretation
  • Build out the Toxicology program and Bio-analytics and biomarker capacity
  • Authoring and review of toxicology sections for regulatory submissions (IND, CTA, NDA/BLA, IBs and CSR)
  • Represent toxicology in cross-functional program teams and governance forums
  • Maintain study timelines and ensure non-clinical studies are conducted in accordance with overall program objectives
  • Assist Non-clinical Project Leaders in integrating and assembling toxicology data for regulatory submissions (e.g., IND, NDA, BLA)
  • Build strong relationships with internal teams and external partners to ensure optimal decision-making

Internal and External Innovation:
  • Partner with key internal experts across the company including Innovation Lab and Business Development (BD) for asset evaluation and development strategies, identify toxicology risks and mitigation strategies
  • Identify and implement innovative AI driven toxicology approaches including NAMs to support regulatory submission and interactions with regulatory agencies

Factors for Success:
Minimum Requirements/Qualifications:
  • PhD, MD/PhD, DVM, or related field in Toxicology, Pharmacology, Biology; DABT or ERT certification preferred.
  • 12+ years in pharma or biopharma toxicology/pathology; preference for individual with experience in ophthalmology.
  • Strong GLP and ICH guidance knowledge; Experience with EMA/FDA CTA/IND submissions and regulatory interactions preferred.
  • Ability to develop comprehensive preclinical safety approaches with internal stakeholders; skilled in executive and agency presentations.
  • Experience managing outsourced studies; thrives in fast-paced environments.
  • Excellent oral and written communication skills, including writing, reviewing, and editing scientific documents.
  • Strong interpersonal skills, diplomacy, and positive-influencing abilities.
  • Exceptional communication, influencing and partnering skills to drive decision-making within a multi-disciplinary, matrix teams.
  • Effective project management skills.
  • Strong presentation skills; must be able to provide succinct, strategic, and actionable insights.
  • Proactive self-starter who can lead work independently, with the ability to see the next step and anticipate issues.
  • Enterprise and entrepreneurial mindset.

Tarsus Competencies:
  • Decision Making - Demonstrates strong decision-making by applying structured analysis to complex challenges, balancing competing priorities and long-term impacts while engaging stakeholders and driving solutions aligned with organizational goals.
  • Collaboration and Team Building - Promotes collaboration by aligning diverse teams around shared goals, fostering healthy debate to advance outcomes, and building strong networks that strengthen organizational effectiveness and cross-team learning.
  • Outcome Driven - Demonstrates strong outcomes focus by aligning teams around shared priorities, proactively addressing risks and dependencies, and driving cross-functional accountability to sustain progress and deliver results.
  • Business Acumen - Demonstrates strong business acumen by anticipating market dynamics and using financial and strategic insight to guide investments, manage risk, and align priorities with long-term organizational value.
  • Innovative Mindset and Action - Demonstrates an innovative mindset by championing new ideas, investing in enabling systems and partnerships, and translating innovation into sustainable growth and organizational resilience.

A Few Other Details Worth Mentioning:
  • The position will be based in our beautiful Irvine office, complete with onsite gym, pool, snacks, drinks, and occasional catered meals. We provide a hybrid work environment. Remote work is an option.
  • We are passionate about our culture! Our Tarsans live our values of commitment to patients, empowerment to champion innovation, and teamwork to amplify impact!
  • This position reports directly to our VP, Translational Science
  • Some travel may be required - up to 20%

At Tarsus, we understand the importance of attracting and retaining top talent. The expected base pay range for this position is $188,200 - $263,600 plus bonus, stock equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training. Our benefits include health, dental and vision insurance benefits to ensure your well-being. We believe in work-life balance and offer generous paid time off, including vacation, holidays, and personal days. For more details regarding Tarsus benefits, please visit: https://eb.alliant.com/26tarsusbenefitssnapshot.
#LI-Hybrid
#LI-Remote
Tarsus Pharmaceuticals, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

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