The Research Assistant assists with the startup and management of clinical trials. The role involves reviewing and understanding research protocols, obtaining clinical trial data, interacting with clinical trial patients, answering trial queries, registering patients in EPIC / CRMS for accurate billing, submitting patient data, maintaining and organizing data for regulatory compliance, preparing ethics board applications, and maintaining study supply inventory. The Research Assistant follows detailed instructions from the research team, works independently within the scope of the clinical trial and instructions from principal investigators, and completes related training such as Human Research Participant Protection and GCP training.
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Job Type
Full-time
Education Level
No Education Listed