Quality Control Reports Coordinator I
Inotiv
September 29, 2026
Full-time
On-site
Evansville, IN
Clinical Research and Development
Role: Quality Control and Report Coordinator I, responsible for reviewing and organizing study data to ensure accuracy, completeness, and compliance with protocols, GLP, SOPs, and regulations. Responsibilities include data quality checks within databases (Provantis, Ascentos), verifying raw data, preparing data tables and study documentation, and maintaining study records. Requirements: Associateβs Degree or higher in sciences or related field, up to 1 year research or QC experience. Skills include proficiency with Windows-based software (Excel, Word, PDF), LIMS systems, and database management. Preferred qualifications are additional experience or education. High-Value: involvement in research quality assurance, data integrity, GLP compliance, laboratory study support, potential exposure to biological hazards, and working in a regulated laboratory environment. Work setup: First shift, on-site; physical activities include prolonged sitting, screen use, and occasional lifting up to 50 lbs.; potential exposure to biohazards and chemicals; environment includes mild to moderate noise levels.