Clinical Records Associate

• Maintain an 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 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

• Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus.
• Thank you.

Kind Regards,

Harris Kaushik

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

• DIRECT # - (650)-399-0891
• Gold Seal JCAHO Certified ™ for Health Care Staffing
• “INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)