Medix™
Job Location : Sarasota,FL, USA
Posted on : 2025-09-01T09:15:17Z
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.