trial to ensure protocol and GCP compliance
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as
up to standard
Required would need to be in the possession of a valid driver’s license with their own transport and have the
in a middle management role in the public health field and HIV/TB Management
in a middle management role in the public health field and HIV/TB Management Experience working in a managerial
in a middle management role in the public health field and HIV/TB Management Experience working in a managerial