The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials. Job responsibilities will include data acquisition with a research device in a clinical setting. Participant recruitment/consenting/interaction, database management, IRB protocol compliance and record keeping. Construction of optical sensors, along with assistance on a variety of other miscellaneous experiments in the lab and clinic. The candidate is expected to be self-motivated, detail oriented, have strong interpersonal skills, and capable of working in a collaborative environment.
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
Number of Employees
5,001-10,000 employees