Clinical Research Coordinator
CurrentResponsible for ensuring the clinical trial meets all regulations & guidelines (Good Clinical Practice)- Patient screening and recruitment,- Monitoring subject’s compliance to their treatment and follow-up,- Facilitate clinical trials in therapeutics of Oncology- 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.