Study Director III, Toxicology

Responsibilities

• Responsible for all phases of protocol development
• Communicate with supervisory staff to establish a study schedule
• Finalize the protocol with the sponsor
• Coordinate study initiation with technical staff
• Direct and/or supervise the work of technical staff
• Monitor the progress of studies and report results to the sponsor
• Participate in in-house training programs for the technical staff
• Conduct literature and/or Internet searches in support of protocol or report preparation
• Prepare posters and/or scientific papers
• Prepare reports, papers, and/or charts of study data
• Prepare interim reports to the sponsor
• Inform management of any issues affecting the conduct of preclinical studies
• Document analytical results
• Adhere to safety regulations and procedures

Requirements

• Bachelor’s degree and 10 years of relevant experience
• Master’s degree and 5 years relevant experience
• Doctoral degree in biological sciences and 2 years relevant laboratory animal experience

Skills And Abilities

• Good organizational skills
• Use of computer to compile and maintain databases
• Knowledge and understanding of cGMP/GLP/GCP and OECD regulations
• Independent work capability
• Written and oral communication skills
• Adherence to safety regulations and procedures

Position Summary

The position involves performing duties of a Study Director.

Benefits

• Health and dental coverage
• Short- and long-term disability
• Paid time off
• Paid parental leave
• 401K

Equal Opportunity Employer

Inotiv is an Equal Opportunity Employer.