Assist CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.Assist with periodic review of study files for completeness. Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.ĭo you want to know more about IQVIA? then see what Forbes said about us!Įssential Functions of a Clinical Trial Assistant (CTA) Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors.Īs a Clinical Trial Assistant within our full-service model, you’ll have the opportunity to embrace your passion for a specific therapeutic area and work with cutting-edge technology developed specifically for CTAs. IQVIA is a leading global provider of contract research services, advanced analytics and technology solutions to the life sciences industry formed through the merger of IMS Health and Quintiles.
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