Clinical Research Coordinator

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 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/ Biomedical Science/ Nursing • 1-2 years of related working or internship experience will be advantageous • Excellent time-management and communication skills • Comfortable with administrative processes • Accurate and meticulous • Able to work independently and as a team • Detail-oriented and self-motivated • Good grasp of MS Office applications