Preclinical Study Coordinator: GLP Compliance & Data Ops
INOTIV BOULDER LLC
Inotiv is seeking a Study Coordinator to support all functions of the preclinical study process. You will communicate with clients, study directors, and technicians, and work in a cross-functional, collaborative team to ensure study timelines and data integrity.
Key duties include submitting materials, coordinating with vendors, maintaining study files, ensuring GLP and regulatory compliance, and assisting with in-life study conduct.
#J-18808-Ljbffr$26 - $31 per hour
...Job Summary The Study Coordinator reports to the Study Coordinator Supervisor... ...all functions of the preclinical study process. The ability to... ...activities Ensure creation of data sheets Confirm lab math... ..., as needed Maintain compliance with all policies and procedures...DataHourly payContract workTemporary workWork at officeFlexible hours$170k - $230k
...chain strategy across preclinical and clinical-stage... ...and ensuring compliance with global regulatory... ...Operations and Data Management on IRT/... ...develop and maintain study-level clinical... ...study execution) Coordinate logistics for preclinical... ...with GMP and GLP regulations and...DataFull timeLive inWork at officeRelocation$136k - $259k
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