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Study
start up for new studies (including protocol review, CRF design,
provide data entry support, generate and review data discrepancy
criteria, provide database design support and conduct User
Acceptance Testing)
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Review
and support the clean up of all clinical data generated from all
ongoing clinical studies
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Participate
in the creation and maintenance of data management
documentation/binders |
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Review
listings for quality, content, format and output |
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Interact
with study team members to define the necessary listings needed for
the support of clean-up, validity and summary tables
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Develop
and perform QC functions on study databases versus Clinical Report
Forms
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