Clinical Research Coordinator - (US-FL-Miami Beach - 33239)

Minimum Education: None
Job Type: Full Time
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Responsibilities : Assesses clinical and financial aspects of potential cardiovascular clinical trials to be done at MSMC.2. Reviews protocol for potential applicability to the target population.3. Prepares Informed Consent Forms based on the local IRB standard format.4. Prepares documents for timely submission to IRB for initial and continuing review of studies and accompany Principal Investigator to IRB meetings, as needed.5. Set up the research registration and billing processes with the hospital administration6. Assesses all aspects of patient eligibility to participate in clinical research projects at MSMC and community physicians' offices7. Obtains informed consent from study related patients in accordance with FDA guidelines8. Coordinates study participants' registration, testing and follow-up scheduling at MSMC and community physicians' offices9. Responsible for receipt and storage of study drug supplies of related studies and responsible for the regulatory compliance of the drug storage rooms.10. Responsible for receipt and storage of investigational devices supplied by different sponsors.11. Performs study related physical examinations, tests, and procedures12. Reports adverse events to MSMC IRB and study sponsor as required by FDA regulations in a timely manner.13. Completes and maintains Case Report Forms (CRFs). Accurately records investigational data according to specific protocols and FDA regulations.14. Maintains electronic databases for the required protocols.15. Creates and monitors databank of potential candidates for upcoming protocols .16. Conducts study in a professional manner with respect to patients' rights and privacy.17. Reviews of study performance, progress, and findings with the principal investigators at regular intervals.18. Communicates effectively with physicians/ancillary staff regarding patient screening and follow-up visits.19. Maintains communication with appropriate research authorities and/or sponsors on research related issues.20. Assists in coordination of financial aspects (i.e. payments, reimbursements, etc) of assigned research protocols.21.  Attends investigator's and coordinator's meetings as needed.

Requirements :Bachelor's Degree required.Computer literacy a must,1 year previous research experienceClinical ServicesResearch TrialsPatient InformationVisitor Information.

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