Study Coordinator

The Study Coordinator will be responsible for supporting all functions of the non-clinical study process. The Study Coordinator will work as part of a team conducting routine procedures required for study conduct; interacting and communicating with clients, study directors, and technicians in a cross-functional, flexible, and collaborative spirit.   Job Summary: The Study Coordinator reports to the Study Coordinator Supervisor with responsibilities centered around supporting all functions of the preclinical study process.  The ability to communicate succinctly with clients, study directors and technicians is key as is a cross-functional, flexible, and collaborative spirit.   Responsibilities: Maintain and submit study initiation materials Communicate effectively with all key stakeholders including vendors and clients Order all applicable supplies for studies Communicate with other coordinators to schedule study activities Ensure creation of data sheets Confirm lab math for test article and disease induction formulation Communicate with formulation department regarding timeline and materials needed Assist with in-life study conduct, as needed, and as trained Complete training requirements as assigned and maintain appropriate training documentation  Perform periodic review of all applicable SOPs to ensure accuracy and confirm procedures are being performed according to SOPs. Participate in SOP writing, reviews, and revisions, as needed Maintain compliance with all policies and procedures Ensure compliance with GLPs, USDA, AAALAC, OLAW and other applicable regulations Perform quality checks, reviews, and formatting on all Inotiv documents (e.g. protocols, amendments, deviations, reports, tables, etc) Develop and maintain protocol, report, and data table master templates Provide back-up support for Study Directors as needed Aid in protocol and any protocol amendment or deviation preparation and distribution Prepare and review raw data collection forms and review for adherence to protocol, both prior to study start and after study completion Review raw data collection and in-life study conduct Assist to prepare a complete study file for archival following finalization of report Assist to ensure that study samples and test articles are shipped appropriately, on schedule, and documented in the study file Perform other duties as assigned Qualifications/Education:   Bachelor's degree in life sciences or other directly related field or degree with comparable coursework and a minimum of 3 years in a relevant pharmaceutical setting One year animal handling experience required Possess strong skills for editing the format, style and language of draft protocols, spreadsheets and reports Experience using Microsoft Office (Word, Excel, Outlook) Excellent written and verbal communication skills An attitude for quality, an eye for detail and the ability to read and follow written instructions Ability…