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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