About this opportunity
Frontage Laboratories, Inc. lists this Associate Director/Director of Toxicology opportunity in chicago, Illinois. Review the employer’s description below for duties, qualifications and application requirements.
Job description
If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.
Associate Director/Director of Toxicology
Full Time Chicago, IL, US
3 days ago Requisition ID: 1840
Salary Range: $140,000.00 To $160,000.00 Annually
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 interpretationExperience 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
Track record of successful client engagement and project delivery
Salary
$140-160k, based upon experience.
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.
#J-18808-Ljbffr
Worksite address
chicago, IL, 60290, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.