ICON plc is Looking to Hire a Global Clinical Project Manager in Qatar تتطلع ICON plc لتوظيف مدير مشروع طبي عالمي في قطر
Global Clinical Project Manager
Responsibilities:
Responsible for Study Management and oversight of all Study Management functions internally and at the CROs
Operational Study Management for 1 or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studies
Accountable for the development of realistic detailed study startup and monitoring plans
Accountable for conducting country level feasibility in collaboration with Global Clinical Trial Execution and CROs, reviewing Pre-trial Assessment outputs , approving sites, and assessing site activation plans
Leads study risk planning process in context of site and subject
Coordinates study/protocol training & investigator meetings
Develops and provides key inputs to Clinical Trial Budget (e.g., Per Subject Costs)
Accountable for the delivery of the study against approved plans
Leads inspection readiness activities related to study management and site readiness
May produce or review model Informed Consent Document (ICD) and study/country/site level ICD, as appropriate
May expand study design document into approved protocol template while incorporating input from other team members (e.g., Clinician, Clinical Pharmacology Lead, Supply Chain Lead, Statistician, Outcomes Research Representative, Clinical Assay Group, etc.)
HOW TO APPLY
To Learn More And To Apply Visit The Following Link
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