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"• Minimum 4 years clinical study database development experience in the pharmaceutical industry 
• Minimum of 3 years hands on Rave study build experience, including module connections such as Safety Gateway and TSDV
• Bachelor's degree required 
• Thorough understanding of regulations, GCP, ICH Guidelines as they apply to creation and maintenance of clinical study databases
• Good ability to communicate with study team members, plan/organize work to deliver against timelines"

"• Build studies for initial deployment and protocol amendments and/or oversee CROs and quality check their work (includes forms, database structures, cleaning edit checks).
• Program study database integrations (TSDV, CCV, TMS, Safety Gateway)
• Work with Data Management/Study teams to plan for build timelines, develop database/edit check specifications, migration content, and migration plans; resolve issues and re-plan as needed
• Serve as a primary database build point of contact for assigned studies and provide support during study execution and closure
• For database changes after initial deployment - perform impact analysis, create test migration plan, execute migration test, and deploy changes into production 
• Support troubleshooting of technical issues, working with other internal groups and with Medidata as needed
• Provide technical support for continuous improvement efforts and audit support (study specific) 
• Build database components at the global level as needed
"

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