Study Director III, Toxicology

Working Conditions: Frequent involvement with radiant/electrical energy, solvents, grease, oil, irritants, acids, bases, and other hazardous chemicals, electro‑mechanical hazards, flammable materials, and biohazards Due to exposure to hazardous biological materials (which may include HIV positive specimens), immunization to diseases may be required Will be exposed to animal dander, bites, scratches, etc., and material associated with animal husbandry Ability to wear latex gloves, dust mask and/or respirator, and safety glasses as required The noise level is usually moderate to loud requiring ear protection Montoux TB test with negative result is required Tools, Equipment, & Other Resources Used Various software applications sustained by a WindowsTM platform (Excel, Word, Power Point, etc.)

Responsibilities and Duties: Responsible for all phases of protocol development; communicating with supervisory staff to establish a study schedule, the sponsor to finalize the protocol, and the technical staff to coordinate study initiation Direct and/or supervise the work of technical staff in accordance with GLP’s Monitor the progress of studies and, after consultation with senior staff, report the 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 With the assistance of senior staff, prepare posters and/or scientific paper that will contribute to the scientific reputation of Inotiv Evansville and the individual In consultation with senior staff, prepare reports, papers and/or charts of study data for interim reports to the sponsor Maintain knowledge of FDA and other regulatory guidelines that may affect protocol development Inform the management of any issues affecting the conduct of preclinical studies, interaction with clients and/or generation of protocols and reports Perform other duties as assigned, maintain confidential information, interact with the community and employees, support and participate in other company initiatives as directed by management

Position Summary: Perform duties of a Study Director, overseeing the production of protocol development, study coordination, and regulatory reporting while ensuring compliance with GLP, cGMP, GCP, and OECD regulations.

Education: Bachelor’s degree and 10years of relevant experience, or Master’s degree and 5years of relevant experience, or Doctoral degree in one of the biological sciences and at least 2years of relevant laboratory animal experience Salary range will adjust along with the level of the role to match the person’s relevant experience and/or education level This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience

Skills and Abilities: Good organizational skills Ability to use a computer to compile and maintain databases for records and inventory, utilizing the appropriate software Knowledge and understanding of cGMP/GLP/GCP and OECD regulations, with the ability to apply these practices daily Ability to work independently Good written and oral communication skills Ability to adhere to all safety regulations and procedures Ability to document analytical results

Benefits: Health and dental coverage Short‑ and long‑term disability Paid time off Paid parental leave 401(k) More benefits as applicable Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.