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Associate Director/Director of Toxicology

0fad767f F389 40ea B2d1 D8df05098476 19000101 000001 · Chicago, IL, US, Chicago, IL · Active · $150,000–$200,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company0fad767f F389 40ea B2d1 D8df05098476 19000101 000001
TitleAssociate Director/Director of Toxicology
Normalized title-
Department / team-
LocationChicago, IL, United States
Work model-
Employment typeFull Time
Salary$150,000–$200,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-05-01 / 2026-05-31
Changed / last seen2026-06-21 / 2026-06-21

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Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Chicago.Open
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Linked records

Company0fad767f F389 40ea B2d1 D8df05098476 19000101 000001
Source57b990c1-73e8-474a-b966-75ea19495511
ATS providerADP Workforce Now Recruiting

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.

Full job record

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Source ID57b990c1-73e8-474a-b966-75ea19495511
Board ID57b990c1-73e8-474a-b966-75ea19495511
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TitleAssociate Director/Director of Toxicology
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CountryUnited States
RegionIL
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Salary Min150,000
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First Seen At2026-05-31 18:30:14Z
Last Seen At2026-06-21 13:25:46Z
Last Checked At2026-06-21 13:25:46Z
Last Changed At2026-06-21 13:25:46Z
Inactive At—
Source Posted At2026-05-01 21:55:00Z
Source Updated At—
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    "requisitionDescription": "<div><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:8.0pt;line-height:115%;' data-pasted=\"true\"><strong><span style=\"font-size: 15px; line-height: 115%; font-family: arial, sans-serif;\">Job Title:</span></strong><span style=\"font-size: 15px; line-height: 115%; font-family: arial, sans-serif;\">&nbsp;Associate Director/Director of Toxicology&nbsp;<br> <strong>Location:</strong> Chicago, IL<br> <strong>Reports to:</strong> Vice President of Safety and Toxicology</span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:8.0pt;line-height:115%;'><span style=\"font-family: arial,sans-serif;\"><strong><span style=\"font-size: 15px; line-height: 115%;\">Full-time</span></strong></span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:8.0pt;line-height:115%;'><span style=\"font-size: 15px; font-family: arial, sans-serif; color: black;\">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.</span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:8.0pt;line-height:115%;'><span style=\"font-size: 15px; font-family: arial, sans-serif; color: black;\">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</span><span style=\"font-family: arial,sans-serif;\"><strong><span style=\"font-size: 15px; color: black;\">.</span></strong></span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:8.0pt;line-height:normal;'><span style=\"font-family: arial,sans-serif;\"><strong><u><span style=\"font-size: 15px;\">Position Summary</span></u></strong><strong><span style=\"font-size: 15px;\">:</span></strong></span><span style=\"font-size: 15px; font-family: arial, sans-serif;\"><br>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.</span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:8.0pt;line-height:normal;'><br></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:0in;line-height:115%;'><span style=\"font-family: arial,sans-serif;\"><strong><u><span style=\"font-size: 15px; line-height: 115%;\">Key Responsibilities</span></u></strong><strong><span style=\"font-size: 15px; line-height: 115%;\">:</span></strong></span></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Lead and oversee General Tox, Developmental and Reproductive Toxicology studies in compliance with GLP and regulatory guidelines&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Provide scientific direction for study design, protocol development, and data interpretation</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Serve as Study Director, as and when needed, or Senior Scientific Advisor on complex programs&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Manage, mentor, and grow a team of Study Directors and scientific staff&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Ensure high-quality deliverables, timelines, and client satisfaction&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Interact with clients to provide scientific guidance and support business development efforts&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Contribute to regulatory submissions and support audits/inspections (FDA, OECD, etc.)&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Stay current with evolving regulatory requirements and scientific advancements&nbsp;</span></li></ul><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:0in;line-height:normal;'><span style=\"font-family: arial,sans-serif;\"><br></span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:0in;line-height:normal;'><span style=\"font-family: arial,sans-serif;\"><strong><u><span style=\"font-size: 15px;\">Qualifications</span></u></strong><strong><span style=\"font-size: 15px;\">:</span></strong></span></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">PhD in Toxicology or a related field&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">5&ndash;7 years of relevant experience in a reputable CRO or pharmaceutical/biotech setting&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Demonstrated expertise in reproductive and developmental toxicology study design and interpretation&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Experience serving as Study Director in GLP-compliant studies&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Proven experience managing and leading scientific teams&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Strong knowledge of regulatory guidelines (FDA, ICH, OECD)&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Excellent communication, leadership, and client-facing skills&nbsp;</span></li></ul><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:0in;line-height:normal;'><span style=\"font-family: arial,sans-serif;\"><br></span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:0in;line-height:normal;'><span style=\"font-family: arial,sans-serif;\"><strong><u><span style=\"font-size: 15px;\">Preferred Qualifications</span></u></strong><strong><span style=\"font-size: 15px;\">:</span></strong></span></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Board certification (e.g., DABT) is a plus&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Experience supporting regulatory submissions (IND, NDA, etc.)&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"font-size: 15px;\">Track record of successful client engagement and project delivery&nbsp;</span></li></ul><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:0in;line-height:normal;'><span style=\"font-family: arial,sans-serif;\"><br></span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:0in;line-height:normal;'><span style=\"font-family: arial,sans-serif;\"><strong><u><span style=\"font-size: 15px;\">Salary</span></u></strong></span><span style=\"font-size: 15px; font-family: arial, sans-serif;\">: $140-160k, based upon experience&nbsp;</span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:0in;line-height:normal;'><span style=\"font-family: arial,sans-serif;\"><br></span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:8.0pt;line-height:normal;text-align:justify;'><span style=\"font-family: arial,sans-serif;\"><strong><u><span style=\"font-size: 15px; color: black;\">Benefits:</span></u></strong></span></p><div style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:115%;font-size:16px;font-family:\"Aptos\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;\"><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"line-height: 107%; font-size: 15px; color: black;\">401k Employer Match with immediate vesting</span></li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"line-height: 107%; font-size: 15px; color: black;\">Vision Insurance&nbsp;</span></li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"line-height: 107%; font-size: 15px; color: black;\">Medical and Dental Insurance with multiple coverage options</span></li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"line-height: 107%; font-size: 15px; color: black;\">FSA (Medical, Dependent Care, and Commuter)</span></li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"line-height: 107%; font-size: 15px; color: black;\">Short Term Disability</span></li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"line-height: 107%; font-size: 15px; color: black;\">Long Term Disability&nbsp;</span></li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"line-height: 107%; font-size: 15px; color: black;\">Life Insurance</span></li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 16px; font-family: arial, sans-serif;\"><span style=\"line-height: 107%; font-size: 15px; color: black;\">Generous Paid Holidays and PTO&nbsp;</span></li></ul></div><p style='margin-right:0in;margin-left:.5in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:8.0pt;line-height:normal;text-align:justify;'><span style=\"font-family: arial,sans-serif;\"><strong><u><span style=\"font-size: 15px; color: black;\">&nbsp;</span></u></strong></span></p><p style='margin-right:0in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;margin-top:0in;margin-bottom:0in;line-height:12.95pt;text-align:justify;background:white;'><em><span style=\"font-size: 15px; font-family: arial, sans-serif; color: black;\">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. </span></em></p></div>\n",
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