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Reproductive Toxicology Jobs (NOW HIRING)

Frontage Laboratories

Director of Toxicology

Chicago, IL · On-site

$150K - $200K/yr

Our Chicago, IL site provides services in General Toxicology, Developmental and Reproductive Toxicology (DART), juvenile and ocular toxicology in support of pharmaceutical and biotechnology products

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How much do reproductive toxicology jobs pay per year?

As of Aug 17, 2026, the average yearly pay for reproductive toxicology 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 are the key skills and qualifications needed to thrive in reproductive toxicology?

To thrive in Reproductive Toxicology, you need a solid background in biology, toxicology, pharmacology, or a related field, typically supported by an advanced degree such as a PhD or master's. Experience with laboratory techniques, regulatory guidelines (e.g., GLP, OECD), and data analysis software like GraphPad Prism or statistical tools is highly valuable. Strong analytical thinking, attention to detail, and clear communication skills help professionals collaborate effectively and interpret complex results. These abilities are crucial for conducting accurate research, ensuring compliance, and providing reliable risk assessments impacting public health and safety.

What is reproductive toxicology?

A reproductive toxicology job involves studying how chemicals, drugs, and environmental exposures affect fertility, pregnancy, and fetal development. Professionals in this field conduct laboratory research, analyze data, and assess potential risks to human and animal reproduction. Their work helps regulatory agencies and industries ensure the safety of pharmaceuticals, consumer products, and industrial chemicals. They may work in academic research, government agencies, or private industry.

What is a reproductive toxicologist?

A reproductive toxicologist is a scientist who studies the effects of chemicals and substances on reproductive health and development. They often work in laboratories, analyzing data and conducting experiments to assess risks, and may require knowledge of biology, toxicology, and regulatory standards.

What are common daily responsibilities for a reproductive toxicologist?

Daily tasks in reproductive toxicology often include designing and conducting experiments to evaluate the effects of chemicals or pharmaceuticals on reproductive systems, analyzing laboratory data, and preparing detailed scientific reports. You may also participate in regulatory submissions, collaborate closely with cross-functional teams such as regulatory affairs, pathology, and analytical chemistry, and stay updated on federal and international safety regulations. The role requires careful documentation and adherence to laboratory safety protocols. Depending on your organization, you might also mentor junior staff or contribute to peer-reviewed publications. This combination of technical and collaborative work makes for a dynamic and impactful career.

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Reproductive Toxicology jobs near you
Infographic showing various Reproductive Toxicology job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 21% Part Time, and 2% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $115,369 per year, or $55.5 per hour.

Director of Toxicology

Frontage Laboratories

Chicago, IL • On-site

$150K - $200K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 17 days ago

Job description

Director, Toxicology


Job Title: Director of Toxicology

Location: Chicago, IL

Reports to: Vice President of Safety and Toxicology


Full-time

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, Europe, and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.


Our Chicago, IL site provides services in General Toxicology, Developmental and Reproductive Toxicology (DART), juvenile and ocular toxicology in support of pharmaceutical and biotechnology products.


Position Summary:

We are seeking an experienced and highly motivated Director of Toxicology with specialized expertise in Developmental and Reproductive Toxicology (DART). 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 scientific staff. The ideal candidate will bring strong scientific expertise, regulatory knowledge, and proven leadership experience within a CRO environment.


Key Responsibilities:

  • Lead and oversee General Tox, Developmental and Reproductive Toxicology studies in compliance with GLP and regulatory guidelines.
  • Provide scientific direction for study design, protocol development, and data interpretation.
  • Serve as Study Director, as and when needed, or Senior Scientific Advisor on complex programs.
  • Manage, mentor, and grow a team of Study Directors and scientific staff.
  • Ensure high-quality deliverables, timelines, and client satisfaction.
  • Interact with clients to provide scientific guidance and support business development efforts.
  • Contribute to regulatory submissions and support audits/inspections (FDA, OECD, etc.).
  • Stay current with evolving regulatory requirements and scientific advancements.


Qualifications:

  • PhD, D.V.M or equivalent in Toxicology or a related field.
  • 10+ years of relevant experience in a reputable CRO or pharmaceutical/biotech setting.
  • Demonstrated expertise in reproductive and developmental toxicology study design and interpretation.
  • Experience serving as Study Director in GLP-compliant studies.
  • Proven experience managing and leading scientific teams.
  • Strong knowledge of regulatory guidelines (FDA, ICH, OECD).
  • Excellent communication, leadership, and client-facing skills.


Preferred Qualifications:

  • Board certification (e.g., DABT) is a plus
  • Experience supporting regulatory submissions (IND, NDA, etc.)
  • Track record of successful client engagement and project delivery


Salary: $150k-$200k, annual salary compensation based on experience.


Benefits:

  • 401k Employer Match with immediate vesting
  • Medical, Dental and Vision Insurance with multiple coverage options
  • FSA (Medical, Dependent Care, and Commuter)
  • Short Term Disability
  • Long Term Disability
  • Life Insurance
  • Generous Paid Holidays and PTO


Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.