Description

Perform duties of a Study Director

Requirements

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’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 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