Contribute to data management activities in support of clinical studies, including:
eCRF development by leading cross-functional reviews of eCRF content
Database build activities, including review of edit check specifications and performance of user acceptance testing
Monitoring data collection, coding, and cleaning by vendors through tracking of study metrics and targeted data reviews
Oversight of database lock activities and ultimate archiving of study data
Collaborate with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Medical, Quality Assurance, Drug Safety and Pharmacovigilance; CROs, central and local laboratories, and other vendors
Establish cross-functional, internal data review plans, coordinate data cuts/transfers, and conduct data reviews
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