What are the responsibilities and job description for the Clinical Research Coordinator 252933 position at Medix™?
Participant Management: Recruit, screen, and consent participants; schedule visits, and monitor patient safety/adverse events.
Protocol Compliance: Implement study protocols and ensure all procedures adhere to FDA, IRB, and GCP regulations.
Data Management: Collect, enter, and maintain accurate, source-documented study data and records.
Regulatory Documentation: Prepare and maintain IRB submissions, investigator files, and regulatory documents.
Study Coordination: Act as a liaison between participants, principal investigators (PIs), sponsors, and study staff.
Logistics: Manage inventory of study supplies and Investigational Product (IP) accountability.
Salary.com Estimation for Clinical Research Coordinator 252933 in Salt Lake, UT
$63,474 to $83,159
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