Jun 04, 2021
This position is to support the Clinical Research Specialist with clinical research organization and implementation. The main focus of this position is to screen potential subjects; recruit patients; obtain informed consent and gather clinical and research data. This position will work closely with the Principal Investigator, resident physicians and other research staff involved in active clinical trials. Additionally, this position will work with clinic staff – including nurses and physicians in the various clinical settings. A large part of this position involves maintaining contact with the research subjects, collecting research data, data entry, building research databases, study start up activities, consent documentation, and maintaining regulatory and IRB documents. This position may cover multiple industry funded, government funded or investigator initiated research studies.
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