*URGENT NEED - MUST HAVE ONCOLOGY*
Responsibilities

+ Coordinate the initiation and activation of new clinical trial protocols, ensuring all required approvals are in place before study activation, including Scientific Review Board, Institutional Review Board, Human Research Oversight Committee, data collection plans, and finance/contract approvals.

+ Prepare and organize study tools such as study binders, medication diaries, eligibility checklists, calendars, and flow sheets as required for each protocol.

+ Use Oncore, Excel, and Word to develop and maintain study tools, including eligibility checklists, medication diaries, calendars, and flow sheets tailored to specific trials.

+ In collaboration with the Research Nurse Clinician and/or physician, review patients’ charts and medical histories to confirm protocol eligibility and obtain necessary source documents from the medical record.

+ Under the direction of the Research Nurse Clinic...