As a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance to the ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act. You will support and assist the Principal Investigator in the following trial related activities: Patient screening and recruitment, Monitoring subject’s compliance to their treatment and follow-up, Data collection and management including resolving data discrepancies, Coordinating the collection of biological specimens, Monitoring of adverse events and safety reporting, Maintaining and organising of investigator site files, preparation and submissions to the ethics committee and relevant local health authorities, Tracking of trial expenditures and timely invoicing. Requirements: Degree in Life Sciences/Nursing OR Diploma in Nursing with minimum 6 years working experience as CRC 2 years of related working experience will be advantageous Excellent time-management and communication skills Able to work independently and as a team Detail-oriented and self-motivated Good grasp of MS Office applications