The Clinical Research Monitor will conduct the site visits for new site membership into the HCRN network, to determine if the sites are qualified to open HCRN clinical trials.
The Clinical Research Monitor will coordinate all aspects of the clinical monitoring process in accordance with Federal Regulations, Good Clinical Practice (GCP), NCI and UCSD SOPs.
The Clinical Research Monitor will monitor trials per HCRN’s Data Safety Oversight Process (DSOP).
The Clinical Research Monitor will travel to HCRN’s sites in accordance with the DSOP for each trial.
The Clinical Research Monitor will complete a monitoring report in HCRN’s EDC system for each visit conducted.
The Clinical Research Monitor will communicate site-level problems with HCRN staff, site study coordinator, and the principal investigator.
Clinical Research Monitoring includes but is not limited to reviewing data collection for accuracy and completeness, training and leading clinical research personnel at centers in protocol procedures and implementation, identifying problems in protocol implementation and conduct, review/resolution of regulatory issues and verify accountability, proper storage, and dispensation records of clinical trial material (CTM).
Bachelor’s degree in science or health related field preferred.
Three years of experience in oncology monitoring.
This position requires the ability to travel 80% of the time.
Job Type: Full-time
Oncology monitoring: 3 years
Required work authorization: