"• Minimum 5 years clinical study database development experience in the pharmaceutical industry
• Minimum of 5 years hands on Rave experience including module connections such as Safety Gateway and TSDV
• Minimum of 2 years hands on experience programming custom functions
• Bachelor's degree required, preferably in computing or scientific discipline
• 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 and plan/organize work to deliver against timelines"
"• Complete DBD I activities and/or complete one or more of the following activities:
• Program custom functions according to best practices
• Liaise with study team/requesters on technical requirements for custom functions
• Lead troubleshooting of technical issues, working with other internal groups and with Medidata as needed
• Provide technical expertise and/or leadership for continuous improvement efforts and audit support (study specific)
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
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