" 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)
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