such as attending to staffing requirements and administration
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
RHI, Department of Health and USAID policies, contracts, and agreements
RHI, Department of Health and USAID policies, contracts, and agreements Support the monitoring, evaluation contribute to achievement Perform and comply with administrative procedures associated with accurate clinical hand Attend to all staffing requirements & administration Supervise & manage the duties of subordinates
RHI, Department of Health and USAID policies, contracts, and agreements Support the monitoring, evaluation contribute to achievement Perform and comply with administrative procedures associated with accurate clinical hand Attend to all staffing requirements & administration Supervise & manage the duties of subordinates