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QC Data Reviewer
3 months ago
- Acts as Lead Data Reviewer for internal studies and works with Study Directors to ensure adequate and timely data review for all aspects of GLP and Preclinical Functionality studies including but not limited to medical records, surgical records, protocols, study data
- Responsible for performing audits of protocol, SOP, and elements of the quality system to ensure preclinical in-vivo studies are compliant to the GLP regulations (21 CFR Part 58) and internal procedures. Adheres to internal quality guidelines.
- Complies with regulations and standards. Identifies basic non-compliance within regulations and standards. Requires excellent attention to detail, a background in data management, and familiarity with medical device GLP research. Requires ability to collaborate among different groups, moving between various locations around the site efficiently and in cooperation with stakeholder schedules.
- Bachelor’s degree with 3 years’ preclinical medical device research experience or 5 years relevant work experience supporting preclinical research (LAR/surgical vet tech).
- Demonstrated understanding in the use of calibrated equipment, controlled drugs, GLP data collection/retention.
