Research Coordinator
Cancer Specialists of North Florida 4.07 reviews - Jacksonville, FL

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Under general supervision, is responsible enlisting and maintaining patients on research protocol regimes. Assists with determining eligibility of patients for clinical trials, presenting trial concepts and details to patients, providing education to staff and patients. Ensuring proper treatment for and assuming responsibility for documentation of patients on protocol.

Essential Duties and Responsibilities:
Screens all physician referred patients for potential protocol eligibility. As directed, presents the trial concepts and details to the patient and obtains informed consent from patient or guardian. Educate patient regarding his/her rights as a research subject. Documents appropriately all components of protocol treatment. Flags medical records with protocol requirements prior to patient appointments. Reviews medical record for toxicity's and dose modifications, when appropriate, in study regimen. Reviews study with patient on an as needed basis. Maintains ongoing communication with patients and physicians regarding progress, side effects and questions. Schedule required tests and treatments and appointments. Orders protocol-required diagnostic studies. Maintains protocol patient database. Ensures accurate data collection, entry, and timely submission to appropriate sponsors.

Education/Experience Graduate from an accredited program in science, or health care related field (BSN Preferred). Experience in medical research preferred.


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About this company
4.07 reviews
Cancer Specialists of North Florida have been involved in clinical trials since 1995 and started as part of the US Oncology Research...