Unmasked Clinical Research Coordinator 243335 Job at Medix™, Sarasota, FL

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  • Medix™
  • Sarasota, FL

Job Description

Key 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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