Job Description
*URGENT NEED - Clinical Research Coordinator – MUST HAVE Oncology*
Responsibilities
+ Lead and coordinate the initiation and activation of new clinical trial protocols, ensuring all pre-activation requirements are complete.
+ Verify approvals from Scientific Review Board (SRB), Institutional Review Board (IRB), Human Research Oversight Committee (HROC), data collection plans, and finance/contract approvals prior to study activation.
+ Coordinate the preparation of study tools, including study binders, medication diaries, eligibility checklists, calendars, and flow sheets, as required.
+ Use clinical trial management systems and Microsoft Excel and Word to develop and maintain study tools and documentation.
+ Collaborate with the Research Nurse Clinician (RNC) and/or physician to review patients’ charts and medical histories to confirm protocol eligibility.
+ Obtain and organize source documents, such as medical record documenta...
Responsibilities
+ Lead and coordinate the initiation and activation of new clinical trial protocols, ensuring all pre-activation requirements are complete.
+ Verify approvals from Scientific Review Board (SRB), Institutional Review Board (IRB), Human Research Oversight Committee (HROC), data collection plans, and finance/contract approvals prior to study activation.
+ Coordinate the preparation of study tools, including study binders, medication diaries, eligibility checklists, calendars, and flow sheets, as required.
+ Use clinical trial management systems and Microsoft Excel and Word to develop and maintain study tools and documentation.
+ Collaborate with the Research Nurse Clinician (RNC) and/or physician to review patients’ charts and medical histories to confirm protocol eligibility.
+ Obtain and organize source documents, such as medical record documenta...
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