Responsibilities: Maintenance of Audit databases (must be very proficient in Word, Excel and Access ) Coordination of GLP audit scheduling Coordination of review and approval of GLP audit reports Scanning and e-mailing of Clinical Packaging/GLP master documentation to external departments and customers Scanning of all completed clinical batch records into shared drive; filing and archival to Cranbury documentation vault Cataloging and sub-cataloging in-process and complex clinical study documentation. Tracking and coordination of all in-process batch records. Maintenance of Clinical Batch Record logbook Maintenance and communication of Departmental review/approval activities Data verification and follow up (GLP Audit findings and Batch Record Review findings) Assist in design and build of template of clinical study protocols Database management and the coordination of the review, approval, scanning, communication and archival of master documentation for the Research QA GLP/Clinical Supply functions Requires 2-4 years related experience,  Bachelors required  Experience:  Maintenance of Audit databases (must be very proficient in Word, Excel and Access ) Coordination of GLP audit scheduling Coordination of review and approval of GLP audit reports Scanning and e-mailing of Clinical Packaging/GLP master documentation to external departments and customers Scanning of all completed clinical batch records into shared drive; filing and archival to Cranbury documentation vault Cataloging and sub-cataloging in-process and complex clinical study documentation. Tracking and coordination of all in-process batch records. Maintenance of Clinical Batch Record logbook Maintenance and communication of Departmental review/approval activities Data verification and follow up (GLP Audit findings and Batch Record Review findings) Assist in design and build of template of clinical study protocols Database management and the coordination of the review, approval, scanning, communication and archival of master documentation for the Research QA GLP/Clinical Supply functions Requires 2-4 years related experience,  Bachelors required