Job Summary

Assist principal investigators and research teams in the conduct / implementation of all aspects of clinical research / clinical trials
Venepuncture, handling and processing of blood samples / human specimens, recording ECG and monitoring vital signs
Ensure all procedures are conducted in accordance with study protocols and regulations
Maintain accurate and complete documentation
Ensure proper storage and dispensing of investigational product (device, drugs, pharmaceuticals)
Liaise with relevant internal and external agencies
Ensure safety of clinical research subjects and report any adverse events to investigators and regulatory authorities

Requirements

Clinical Research Co-ordinator

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