activities Review and ensure essential regulatory documentation available and up to date across all studies Operating Procedures (SOPs), and Regulatory Essential Documents per sponsor requirements Coordinate staff training studies and SOPs, knowledge of clinical research documentation Computer literate with the ability to create
activities Review and ensure essential regulatory documentation available and up to date across all studies Operating Procedures (SOPs), and Regulatory Essential Documents per sponsor requirements Coordinate staff training studies and SOPs, knowledge of clinical research documentation Computer literate with the ability to create
VAT regulations in terms of external supporting documents and Supplier tax invoices Review all sundry payments
VAT regulations in terms of external supporting documents and Supplier tax invoices Review all sundry payments
VAT regulations in terms of external supporting documents and supplier tax invoices Accurately process sundry
Procurement and HR Develop and maintain an effective document management system for the programme Conduct training ongoing basis Develop and maintain an effective document management system Provide full administrative
Procurement and HR Develop and maintain an effective document management system for the programme Conduct training ongoing basis Develop and maintain an effective document management system Provide full administrative
source documents, designing and reviewing protocol-specific forms and study-related documents Liaise Oversee maintenance and deployment/use of study documents and files (e.g. regulatory files/Investigator
source documents, designing and reviewing protocol-specific forms and study-related documents Liaise Oversee maintenance and deployment/use of study documents and files (e.g. regulatory files/Investigator
activities Quality control CRFs and other study documents Safekeeping of project assets Facilitate training