Clinical Research Coordinator 252933 (Salt Lake City)
Medix™, Salt Lake City, UT, United States
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.
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.