Study Director III, Toxicology

Location: Mount Vernon

Performance requirements

Characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

General Ability to read, write, speak, and understand English Ability to read, write and understand oral and/or written instructions

Physical Activity Ability to read, write and interpret scientific material

Manual dexterity to perform research functions, type and use office equipment

Ability to stand or sit for long period of time 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 a required

Will be exposed to animal dander, bites, scratches, etc., and material associated with animal husbandry

Able to wear latex gloves, dust musk and/or respirator, and safety glasses as required.

The noise level is usually moderate to loud requiring ear protection

Mantoux TB test with negative result is required

Tools, Equipment, & Other Resources Used Various software applications sustained by a WindowsTM platform. (Excel, Word, PowerPoint, 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 the GLP’sMonitor 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

Position Requirements Education and experience

This position requires a bachelor’s degree and 10 years of relevant experience, or a master’s degree and 5 years relevant experience, or a doctoral degree in one of the biological sciences and at least 2 years relevant laboratory animal 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

Know and understand cGMP/GLP/GCP and OECD regulations, as applicable, 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

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. The salary range will adjust along with the level of the role to match the person’s relevant experience and/or education level.

Inotiv is a growing contemporary drug discovery and development company where we “Play to Win” in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There’s an opportunity for everyone at all phases of a career, each…