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Pharmaceutical Toxicologist Jobs (NOW HIRING)

ITG Brands

Toxicologist

Greensboro, NC · On-site

$138K - $184K/yr

... pharmaceutical, or consumer products). Certification: Diplomate of the American Board of Toxicology ... DABT) strongly preferred; candidates should be willing to obtain if not already certified.

ITG Brands, LLC

Toxicologist

Greensboro, NC · On-site

$138 - $185/hr

... pharmaceutical, or consumer products). Certification: Diplomate of the American Board of Toxicology ... DABT) strongly preferred; candidates should be willing to obtain if not already certified.

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How much do pharmaceutical toxicologist jobs pay per year?

As of Sep 3, 2026, the average yearly pay for pharmaceutical toxicologist 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.

What does a pharmaceutical toxicologist do?

A Pharmaceutical Toxicologist studies the safety and effects of drugs, chemicals, and other substances on biological systems. They assess potential risks, determine safe dosage levels, and help ensure regulatory compliance for new pharmaceuticals. Their work involves laboratory testing, data analysis, and collaboration with regulatory agencies to protect public health.

What skills and qualifications are needed to be a pharmaceutical toxicologist?

To thrive as a Pharmaceutical Toxicologist, you need a strong background in biology, chemistry, or pharmacology, typically supported by an advanced degree in toxicology or a related field. Proficiency with laboratory instrumentation, toxicological databases, and adherence to regulatory guidelines such as GLP and the ICH are essential. Excellent analytical thinking, attention to detail, and written and verbal communication skills help you collaborate effectively and convey complex findings. These competencies ensure safety and regulatory compliance in pharmaceutical product development.

What challenges do pharmaceutical toxicologists typically face in the workplace?

Pharmaceutical Toxicologists often face challenges such as interpreting complex toxicological data, designing robust studies under tight deadlines, and ensuring strict compliance with evolving regulatory standards. They may also encounter difficulties in communicating complex scientific findings to cross-functional teams or regulatory authorities. Successfully overcoming these challenges requires strong problem-solving abilities, adaptability, and ongoing collaboration with researchers, regulatory experts, and project managers. These aspects make the role both intellectually stimulating and crucial to the safe development of pharmaceuticals.

Are pharmaceutical toxicologists in high demand?

Pharmaceutical toxicologists are in steady demand due to their role in ensuring drug safety and regulatory compliance. Employment opportunities are often available in pharmaceutical companies, research institutions, and regulatory agencies, especially for those with strong analytical skills and relevant certifications.

Do pharmaceutical companies hire pharmaceutical toxicologists?

Yes, pharmaceutical companies often hire pharmaceutical toxicologists to assess the safety and toxicity of new drugs during development. These professionals typically work in research and development, utilizing skills in toxicology, laboratory testing, and regulatory compliance to ensure drug safety before approval.
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Pharmaceutical Toxicologist jobs near you
Infographic showing various Pharmaceutical Toxicologist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $115,369 per year, or $55.5 per hour.

Senior Toxicologist

Regeneron Pharmaceuticals, Inc (USA)

Cambridge, MA • On-site

$140 - $210/hr

Other

Posted 16 days ago

Regeneron rating

8.5

Company rating: 8.5 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

19th of 86 rated pharmaceutical

Job description

Senior Toxicologist

The Senior Toxicologist utilizes their scientific expertise and regulatory experience to lead nonclinical development programs with guidance from their direct supervisor working effectively within cross‑functional project teams. The Senior Toxicologist will demonstrate a thorough understanding of GLP regulations and FDA/EMEA/ICH nonclinical safety guidelines to independently lead the design, conduct, interpretation, and reporting of regulatory toxicology and/or exploratory pharmacology/toxicology studies in rodent and non‑rodent safety models. The Senior Toxicologist will provide primary authorship of all regulatory documentation required for submission packages, demonstrating excellent problem‑solving and communication skills (written and verbal). Experience with multiple therapeutic modalities preferred, including antibody, oligonucleotide, and gene‑therapy products.

Responsibilities
  • Represent toxicology on global research and development project teams communicating non‑clinical safety assessment strategy.
  • Coordinate cross‑department execution of the experimental plan including program budgets, and timing of toxicology studies in relation to regulatory and clinical milestones.
  • Work with the study monitoring group to coordinate, design, monitor, and report toxicology and safety pharmacology studies at contract research organizations.
  • Communicate toxicology study findings, including relevant interpretation, to project teams and management.
  • Contribute to non‑clinical sections of regulatory documents including IND and NDA submissions.
  • Maintain currency with GLP regulations and ICH, FDA and EMEA non‑clinical safety guidelines.
  • Keep up with the latest scientific developments by reading the current literature and attending conferences.
Requirements
  • Advanced degree (e.g. PhD, DVM) in pharmacology, toxicology or closely related biological science along with 3-5 years relevant pharmaceutical industry experience.
  • Or Master’s Degree + ≥10 years relevant pharmaceutical industry experience in designing, monitoring and interpreting non‑clinical safety studies.
Equal Opportunity Employment

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

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