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Job Overview
Entry of clinical data into Clinical Data Management Systems and administration of documents to produce efficient, quality data management products that meet customer needs.

Essential Functions
• Perform the role of Data Entry Associate, File room Associate, Scanning Associate, Indexing Associate, or other role as defined by manager. Process, log, and track clinical study documents in accordance with CRF Tracking and Data Entry Guidelines. Process and enter data accurately and in a timely manner in accordance with CRF Tracking and Data Entry Guidelines. Understand and comply with core operating procedures and working instructions. Assist in the maintenance of Data Management Study files. Meet objectives as assigned. Develop and maintain good communications and working relationships within CDM team.

Qualifications
• High School Diploma or equivalent  Req
• Equivalent combination of education, training and experience in lieu of degree.
• Good organizational and communication skills. Excellent computer skills. Ability to exercise excellent attention to detail. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Good organizational and communication skills. Excellent computer skills. Ability to exercise excellent attention to detail. Ability to establish and maintain effective working relationships with coworkers, managers and clients.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com