This position works with the study physician to ensure all patients involved in a clinical research trial are managed safely and effectively throughout their episode of care and participation in the trial. The role involves managing all elements of a clinical research trial to meet protocol obligations while adhering to regulations, including Code of Federal Regulations Good Clinical Practices (GCP), International Conference on Harmonization GCP guidelines, state regulations, and departmental/institutional standard operating procedures.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree