Unmasked Clinical Research Coordinator 243335 at Medix™ Sarasota, FL
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.
• 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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