Clinical Research Assistant 251270
Medix™
A Clinical Research Assistant supports medical researchers in planning and executing clinical trials. They perform essential administrative duties, manage study documentation, screen participants, and assist with data entry to ensure trials run ethically and smoothly. Core Responsibilities Participant Management: Assist with recruiting, pre-screening, and scheduling study participants for trial visits. Data Entry: Transfer participant information and clinical trial data into approved Electronic Data Capture (EDC) systems with high accuracy. Regulatory Compliance: Maintain study binders, organize regulatory documents, and help assemble submission packets for the Institutional Review Board (IRB). Laboratory Assistance: Prepare, label, and process biological samples (e.g., blood) and organize study supplies. Participant Support: Welcome patients, answer their questions, and ensure they are comfortable during trial visits. #J-18808-Ljbffr Medix™
Vacancy posted 1 day ago
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