DART Study Director – GLP Regulatory Studies

Frontage Laboratories, Inc; Chicago (IL); On-site; USD 95,000 - 130,000; Full time

Benefits offered by this job

401k Plan with employer match

Vision Insurance

Medical and Dental Insurance

FSA (Medical, Dependent Care, and Comm

Long Term Disability

Life Insurance

Paid Holidays and PTO

Job summary

Frontage Laboratories, Inc. is seeking a Study Director for Developmental and Reproductive Toxicology (DART) to lead nonclinical studies and oversee regulatory submissions in Chicago.

The role emphasizes GLP compliance, cross-disciplinary leadership, and client interactions to ensure robust study conduct and reporting. The successful candidate will manage Embryo-fetal Development, Fertility, Pre-/Postnatal and Juvenile Toxicology studies, collaborating with global teams and external clients to

Qualifications

• PhD in toxicology or a related field; DABT preferred but not required.
• MS with 2+ years of relevant scientific experience.
• BS with 5+ years of relevant scientific experience.
• Ability to work across multiple disciplines and manage multiple projects.
• Excellent written and verbal communication skills.
• Thorough understanding of GLP regulatory requirements.
• Knowledge of SOPs and IACUC requirements.
• Demonstrated leadership and client interaction experience.
• Proficiency with Excel, Word, PowerPoint and standard lab calculations.

Responsibilities

• Direct nonclinical DART studies and regulatory submissions.
• Design study protocols, evaluate data and report results per GLPs.
• Stay current with DART study designs and techniques.
• Review external, visceral and skeletal fetal abnormalities.
• Prepare study-specific methodologies and SOPs as needed.
• Provide expert consultations to clients on DART study designs and timings.

Skills

Leadership

Client interactions

Study design

GLP knowledge

Communication

Microsoft Office

Education

PhD in toxicology

Master’s degree

Bachelor’s degree

Tools

Excel

Word

PowerPoint

Job description

Frontage Laboratories, Inc. is seeking a Study Director for Developmental and Reproductive Toxicology (DART) to lead nonclinical studies and oversee regulatory submissions in Chicago.

The role emphasizes GLP compliance, cross-disciplinary leadership, and client interactions to ensure robust study conduct and reporting. The successful candidate will manage Embryo-fetal Development, Fertility, Pre-/Postnatal and Juvenile Toxicology studies, collaborating with global teams and external clients to