Unmasked Clinical Research Coordinator 243335 at Medix™ Sarasota, FL

Medix™

Sarasota, FLFull-timePosted Apr 7, 2026

Behavioral Health Market Context

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Job Description

uments.
• Schedule participant visits, perform informed consent discussions, and ensure participant safety and protocol compliance.
• Monitor and report adverse events in accordance with trial protocols.
• Communicate with sponsors, monitors, and internal teams.
• Assist in inventory and accountability of investigational products.
• Ensure proper documentation of unblinded processes and adherence to GCP (Good Clinical Practice) guidelines.

Qualifications

    Benefits

      Responsibilities

      • Coordinate day-to-day operations of clinical trials in accordance with study protocols and regulatory requirements
      • Maintain knowledge of treatment assignments and ensure appropriate handling of unblinded information
      • Collect and document source data, case report forms (CRFs), and regulatory documents
      • Schedule participant visits, perform informed consent discussions, and ensure participant safety and protocol compliance
      • Monitor and report adverse events in accordance with trial protocols
      • Communicate with sponsors, monitors, and internal teams
      • Assist in inventory and accountability of investigational products
      • Ensure proper documentation of unblinded processes and adherence to GCP (Good Clinical Practice) guidelines


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