Clinical Research Coordiantor
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POST DATE 9/6/2016
END DATE 12/19/2016
Provides assistance in the collection and processing of research data in support of System physicians' clinical trials. May collect and record data in strict accordance with specified research and clinical protocol. May travel to various sites within a specified geographical area, as appropriate to the objectives of the study.
Assists in literature search, protocol writing, case report form design, and IRB submission for new research studies.
Develops visit schedules; contacts potential subjects to introduce and explain study objectives and protocol, and to arrange appointments, either in person or by telephone. Performs subject recruitment, and subject scheduling, for identified clinical trials. Coordinates and conducts clinical research subject visits.
Collects, processes, and assists in the compilation and verification of research data, following strict protocol and detailed instructions.
Assists with routine data analysis and interpretation, as specifically assigned; may utilize statistical data analysis programs and software.
Assists with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol.
Required: Experience in a Clinical Research setting, with at least two years of experience managing oncology trials and/or inpatient trials.
Preferred: 3-5 years of experience in oncology trials