The Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries.
Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information;
present this information at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities.
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
Clinical Research Coordinator
Nursing, Biology, Public Health)Minimum of 1 year of experience in clinical researchKnowledge of Good Clinical Practice (GCP), FDA regulations, and IRB processesExperience with electronic medical records (EMR) systems is a plusCertification in clinical research (e. A company is looking for a Clinica...
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