Clinical Research Coordinator
3 weeks ago
- Screens all physician referred patients for protocol eligibility and as directed, presents the trial details to the patient, and obtains informed consent from the patient or legal guardian
- Educates the patient regarding his/her rights as a research subject
- Documents appropriately all components of protocol treatment, and ensures accurate data collection, entry and timely submission to appropriate sponsors
- Schedules required tests and treatments and appointments, orders required diagnostic studies, and maintains protocol patient database
- Reports patient progress and submits data to the sponsor per protocol; assesses patient for changes in condition
- Facilitates dosage modification by assessing patient, patient labs, consulting protocol or treatment plans, calculating doses, and reporting to physicians
- Participates in drug accountability activities for protocols
- Anticipates and orders appropriate study medication and supplies for efficient management of protocol
- Promotes and educates clinical staff and physicians concerning the protocol studies available to patient enrollment and acts as a resource for clinical staff and patients/families regarding protocol questions
- All other duties as assigned
Location Address: 700 3rd Street, Neptune Beach, FL 32266
Education and/or Experience:
- Graduated from an accredited program in science or a healthcare-related field, BSN preferred
- Experience in medical research, oncology experience preferred
- PharmD preferred
- Nursing experience preferred
- Salary is commensurate with experience and qualifications
Cancer Specialists of North Florida is an "EEO Employer" and "Drug Free Workplace"
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