Frontage Laboratories

Study Director, Toxicology

Frontage Laboratories • $85K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in toxicology or related area; DABT certification preferred but not mandatory.
  • Relevant experience considered in lieu of PhD.
  • Master’s degree with 2+ years of relevant scientific experience.
  • Bachelor's degree with 5+ years of relevant scientific experience.
  • Strong ability to manage multiple projects across various disciplines.
  • Effective written and verbal communication skills.
  • Comprehensive understanding of GLP regulatory requirements and toxicology guidelines.

Responsibilities

  • Direct nonclinical toxicology studies for regulatory submissions, ensuring compliance with GLPs.
  • Develop study designs and protocols, alongside data evaluation and reporting.
  • Stay updated with current Safety and Toxicology study designs and methodologies.
  • Prepare study-specific methodologies and standard operating procedures (SOPs).
  • Provide expert consultations to clients regarding IND enabling toxicology studies.

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 and Long Term Disability
  • Life Insurance
  • Generous Paid Holidays and PTO
Full Job Description
Study Director

Title: Study Director; Toxicology

Location: Chicago, IL (on-site)

Reporting to: VP of Toxicology

Full-time

Our Chicago, IL site provides toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products.

We have an excellent career opportunity for a Study Director - Safety and Toxicology to join our dynamic team inChicago!

Position/Job Summary: This position is fora Study Director within the Safety and Toxicology department at Frontage, specifically to perform duties related to directing nonclinical Toxicology studies in as Study Director for regulatory submissions. The person will serve as the Study Director for Toxicology Studies, including Non-GLP MTD/DRF, and Acute, Sub-Chronic and Chronic GLP Toxicology Studies as described. They have overall responsibility for the technical conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results. Activities also include productive interactions with management, technical staff, global internal and external clients, and study direction staff.

Roles & Responsibilities:
  • Perform responsibilities as a Study Director for regulatory and exploratory toxicology studies, including study design and protocol development, as well as data evaluation and reporting in compliance with GLPs.
  • Stay current with Safety and Toxicology study designs and techniques.
  • Prepare study specific methodologies and SOPs, as needed.
  • Trained in providing expert consultations to clients on IND enabling toxicology studies.


Education, Experience & Skills Required:
  • PhD in toxicology or related subject, DABT certification preferred but not required.
  • Relevant experience may be accepted in place of a PhD.
  • Masters with 2+ years of relevant scientific experience.
  • Bachelor of Science with 5+ years of relevant scientific experience.
  • The ability to work across multiple disciplines and to manage multiple projects simultaneously is highly desirable.
  • Effective written and verbal communication skills required.
  • Thorough understanding of GLP regulatory requirements, and various toxicology testing guidelines.
  • Knowledge of standard operating procedures and IACUC requirements.
  • Demonstrated leadership skills, experience with client interactions and business development.
  • Proficiency in the use of standard software including Microsoft Excel, Word, PowerPoint, etc. and with standard laboratory calculations.
  • The company offers a competitive package of benefits including health insurance, 401K Plan and profit-sharing.


Salary: $85K-$120K, negotiable based on qualification and 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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