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.