Clinical Documentation Jobs in Riyadh

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) tea...

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) tea...

Job DescriptionThis role combines the accountability of a clinical research manager and certain elements of a GCTO country lead role. Holders of this position are accountable for:The performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations Our...

Job Description SummaryThe SSO Study StartUp Manager is accountable for study planning SSU activities and activation deliverables of assigned projects in compliance with Novartis processes GCP/ICH and regulatory requirements in a standalone country OPC (operating country) or satellite country. Leads...