Configure eSource, EDC, Laboratory Information Systems, and other clinical systems based on study protocols, laboratory manuals, pharmacy manuals, and related study documentation.
Create and maintain CDISC/CDASH-compliant eCRFs, study workflows, dynamic forms, and conditional logic.
Perform comprehensive quality review of bioanalytical assay data for accuracy, completeness, data integrity, and compliance with GLP/GCP requirements, study protocols, SOPs, and client expectations.
Review datasets generated from method development, method validation, and sample analysis studies.
