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Associate Reproductive Toxicology Jobs (NOW HIRING)

GSK

Associate Director Toxicology

Upper Providence, PA · On-site

You will lead reproductive toxicology activities that support the safe and timely progression of ... Key responsibilities for the Associate Director Toxicology include: This role will provide YOU the ...

Corteva Agriscience

Study Coordinator

Newark, DE · On-site

The Team Lead, In Vivo Associate Investigators will provide hands-on people leadership and ... reproductive (DART), and general toxicology study conduct, including endpoints and sample ...

Uofl

... reproductive health; racial-ethnic, gender and geographic health disparities; global health; the ... toxic nanoparticle exposures on health; interactions among genetic, behavioral societal and ...

Rutgers University

Post-Doc Schindler Lab

Piscataway, NJ · On-site

$63K/yr

The laboratory research uses mouse systems to study processes relevant to human reproduction using ... Work involves possible exposure to malodorous vapors and toxic chemicals. Long periods of standing ...

All JobsAssociate Reproductive Toxicology Jobs

Associate Reproductive Toxicology information

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$53K

$111.7K

$171K

How much do associate reproductive toxicology jobs pay per year?

As of Jul 7, 2026, the average yearly pay for associate reproductive toxicology in the United States is $111,745.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $137,000.00 per year, depending on experience, location, and employer.
What are the most commonly searched types of Reproductive Toxicology jobs? The most popular types of Reproductive Toxicology jobs are:
Associate Reproductive Toxicology jobs near you
Infographic showing various Associate Reproductive Toxicology job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $111,745 per year, or $53.7 per hour.
Associate Director/Director of Toxicology

Associate Director/Director of Toxicology

Frontage Laboratories

Chicago, IL • On-site

$150K - $200K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 days ago

Job description

Job Title: Associate Director/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:
Frontage Laboratories is seeking an experienced and highly motivated Director of Toxicology with specialized expertise in Developmental and Reproductive Toxicology. This leadership role will be responsible for overseeing study design, execution, and interpretation of nonclinical toxicology studies, while managing and mentoring a team of scientists. 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 in Toxicology or a related field
  • 5–7 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: $140-160k, based upon experience


Benefits:

  • 401k Employer Match with immediate vesting
  • Vision Insurance
  • Medical and Dental 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.