Clinical Investigational Drug Management
Manage preparation, receipt, dispatch and storage of Clinical Investigational Drug (CID)
Type
Domain
Competency Area
Drug Compounding and Management
Levels
Manage Clinical Investigational Drug (CID) products including inventories and records
Retrieve CID records upon receipt of orders
Prepare CID according to study protocols
Store CID according to study protocols and Singapore Guideline for Good Clinical Practice (SG-GCP)
Conduct cycle count of CID
Investigate reasons for discrepancies between physical count and system quantity
Liaise with suppliers for drug replacement and return procedures and inform pharmacists
Review Clinical Investigational Drug (CID) workflows
Identify redundant and improvement areas on CID inventories and drug accountability logs
Monitor the use of CID
Manage the return or disposal of CID and study materials according to study protocols
Maintain CID databases
Implement systematic filing systems
Fill in information into clinical trial accountability logs for shipment receipt and destruction
Distribute CID to the clinical trial teams
Identify areas of improvements and redundancies
Analyse existing CID workflows
Conduct improvement projects for CID-related workflows
Adhere to regulatory requirements in the disposal of pharmaceutical waste
Resolve CID dispensing records discrepancies