Posted in Other about 3 hours ago.
GENERAL SUMMARY/ OVERVIEW STATEMENT:
The Clinical Research Coordinator (CRC I) works under general supervision and reports to the physician leadership for day-to-day responsibilities and to the MGH Cancer Center Protocol Office (CCPO) Clinical Research Manager for administrative aspects. The CRC I will assist in the management of multiple tissue banking protocols.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
The following job duties will be performed under general supervision:
• Have comprehensive knowledge of all assigned protocols
• Develop protocol specific flow charts, intake sheets and other tools as needed to ensure protocol compliance and proper data acquisition
• Assist in the identification and organization of collected samples
• Attend research focused team meetings
• Maintain accurate patient research files and records of sample procurement
• Build and maintain RedCap database of all patients
• Prepare and submit protocol amendments and continuing reviews to the designated Institutional Review Board (IRB) for all assigned protocols
• Obtain consent from patients to collect and analyze data to ensure quality
• Work with collaborators to collect and analyze data to ensure quality
• Other projects as identified by physician leadership
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