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 with the ICH Good Clinical Practice guidelines, as well as 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 of subject’s compliance to their treatment and follow-up,
• Data collection and management including resolving data discrepancies,
• Management of biological specimens (where applicable),
• Monitoring adverse events and safety reporting, maintaining and organising the investigator site files, as well as preparation and submissions to the ethics committee and where applicable, to the relevant local health authorities,
• Tracking of trial expenditures and timely invoicing (where applicable), etc. 

Requirements:

• Degree in Life Sciences/Nursing, or Diploma in Nursing with minimum 6 years working experience as a CRC
• 2 years of related working experience would be an added advantage
• Good time-management and communication skills
• Able to work independently and is detailed oriented
• Computer literate