Cancer Prevention Trials Unit, Barts and the London Medical School
Management of specimens from a live clinical trial including logistical client support of 215 trial sites across 15 countries. Responsible for resupply, courier, storage and other related queries.
Point of contact for and management of external laboratories. Acted as interface between investigator sites, external and internal laboratories and trial management. Including organising analysis and reporting of results with investigation of related deviations or issues. Responsible for authoring and reviewing of lab based SOP’s to ensure good quality data. Data cleaning (and support of data managers) of results of
analysis as required for periodic database lock.
Responsible for updating clinical trial databases and providing regular reports to management to identify and solve any identified issues. Setup automated email management reporting to identify site related specimen and compliance issues.
Joint lead on site wide specimen tracking project – awarded funding for sample and results tracking system with barcoding capability. Responsible for staff training using the new system.
Actively working to GCP, GCLP and HTA regulation.