Frontage Laboratories

Associate Director/Director of Toxicology

Frontage Laboratories$140K — $160K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • PhD in Toxicology or a related field
  • 5-7 years of relevant experience in a CRO or pharmaceutical/biotech setting
  • Expertise in reproductive and developmental toxicology study design
  • Experience as Study Director in GLP-compliant studies
  • Proven leadership in managing scientific teams
  • Strong knowledge of FDA, ICH, OECD regulatory guidelines
  • Excellent communication and client-facing skills

Responsibilities

  • Lead and oversee toxicology studies in compliance with GLP and regulations
  • Provide scientific direction for study design and data interpretation
  • Serve as Study Director or Senior Scientific Advisor as needed
  • Manage and mentor a team of Study Directors and scientific staff
  • Ensure high-quality deliverables and client satisfaction
  • Interact with clients to provide scientific guidance and support business development
  • Contribute to regulatory submissions and support audits/inspections
  • Stay current with regulatory requirements and scientific advancements

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
Full Job Description
Job Title: Associate Director/Director of Toxicology
Location: Chicago, IL
Reports to: Vice President of Safety and Toxicology

Full-time

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


About Frontage Laboratories

Frontage Laboratories is a contract research organization (CRO) that provides research and development services to pharmaceutical and biotechnology companies. The company was founded in 2001 and is headquartered in Malvern, Pennsylvania. Frontage Laboratories offers a wide range of services including drug discovery, preclinical and clinical development, bioanalysis, and regulatory affairs. The company has facilities in the United States and China. Frontage Laboratories is known for its expertise in drug development and its ability to provide customized solutions to its clients.
Learn more about Frontage Laboratories
Size
1,000 employees
Industry
Founded
2001

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