GENERAL SUMMARY / OVERVIEW STATEMENT:
The Program for the Coordination and Oversight of Research Protocols (PCORP) within the MGH Cancer Center Protocol Office specializes in the central coordination, monitoring and regulatory oversight of Investigator-initiated, multi-center clinical trials. PCORP is seeking candidates experienced in clinical trial implementation to coordinate and monitor multiple oncology trials.
The Multi-Center Clinical Research Associate/Monitor III (CRA III) works independently, under minimal supervision, to initiate, manage and navigate a portfolio of Investigator-initiated, multi-center clinical research trials. Specifically, the CRA III will carry out the activation, training, monitoring and oversight of participating institutions while also supporting and ensuring compliance with the regulatory responsibilities of the Sponsor Investigator. This role focuses on centralized trial coordination and does not include direct patient contact.
Trial and portfolio coordination