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Organization / Workplace
India India
Occupation
Clinical Research Coordinator
About
Administering the process of the informed consent to the potential study subjects and discussing in detail with them, the patient information sheet.
Ensure the fulfillment of all the inclusion and exclusion criteria.
Maintain all the study related logs – screening, enrollment and other communication logs, including forwarding all relevant logs to Sponsor in a timely manner.
Schedule subject visit as per the protocol.
Coordinate all lab related activities – shipment of samples through the designated courier and ensure timely receipt of the lab reports
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