Quality Control and Reports Coordinator I

Role: Quality Control and Report Coordinator Level I responsible for reviewing, Quality Checking, and organizing raw and electronic study data to ensure accuracy, completeness, and compliance with protocols, GLP, SOPs, and regulations. Responsibilities: perform detailed data reviews within databases (Provantis, Ascentos), verify raw data findings, compile Data Tables, and maintain facility records. Collaborate with departments and participate in study initiation. Requirements: associate’s degree or higher in sciences, up to 1 year of research or QC experience, strong organizational and attention-to-detail skills, proficiency with Microsoft Office, Adobe PDF, and laboratory data systems. Preferred qualifications are not specified. High-value: supporting GLP-compliant research data management in preclinical studies, exposure to laboratory software tools, working in an environment with biological materials, and potential exposure to biohazards or chemicals. Work setup: primarily office-based with sit/stand activities, potential for overtime, possible exposure to biological and chemical hazards, with physical activity involving prolonged screen time and handling of laboratory materials.