This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
Clinical Records Associate
Maintain a minimal understanding of GCP, ICH and GLP regulations associated with the maintenance and retention of clinical trial documentation and preclinical study records. Participate in continued security and maintenance of the Trial Master File (TMF) Room. Participate in offsite storage activates. Create and maintain study specific file structures for Gilead clinical, biometrics, and preclinical documents and file documents accordingly. Ensure record filing is kept up to date and is performed accurately. Perform an inventory review for incoming CRO clinical study files; receive, index, and file preclinical study records; responsible for offsite archival of documents; participate in periodic file room utilization reviews; file incoming documents and retrieve documentation from the TMFR upon request. May provide support during TMF-related regulatory agency and internal GCP inspections readiness. Assist in the development of electronic tracking/filing systems
Worksite address
foster city, CA, 94420, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.