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GENERAL DESCRIPTION:
The Program for the Coordination and Oversight of Research Protocols (PCORP) within the MGH Cancer Center Protocol Office specializes in the monitoring and regulatory oversight of Investigator-initiated, multi-center clinical trials. PCORP is seeking candidates to monitor oncology trials.
The Multi-center Clinical Research Associate/Monitor works under general supervision to provide regulatory oversight and monitoring for a portfolio of Investigator-initiated, multi-center clinical research trials. The Monitor position ensures Sponsor and site regulatory adherence, verifies source documentation, monitors data quality and completeness and assesses protocol compliance across participating trial sites. The role focuses on trial quality assurance and does not include direct patient contact.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
Principal responsibilities include:
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