Teams at eClinical Solutions

Manages clinical data throughout the study lifecycle, including protocol conversion, database builds, CRF design, data review, query management, reporting, and quality control. Collaborates with sponsors, clinical operations, biostatistics, programming, and technical teams to configure data-cleaning strategies, monitor KPIs, identify risks, and ensure compliant, timely deliverables. Provides project leadership, develops study documentation, performs trending analysis, and supports continuous process improvement.

Processes and quality-checks external and local laboratory data throughout clinical trials. Reviews protocols, eCRF designs, vendor data transfers, normal ranges, reconciliation logs, exception listings, and clinical database alignment. Supports study start-up, data documentation, issue resolution, reporting, metrics, and vendor agreements while ensuring ICH/GCP, SOP, and data integrity standards. Collaborates with clinical data management, project teams, clients, laboratories, and vendors.

Perform centralized medical coding and serious adverse event reconciliation for clinical trials. The role maintains coding guidelines and SAE plans, codes using MedDRA and WHODrug, reviews coding accuracy, resolves discrepancies with clinical and safety teams, documents decisions, supports dictionary versioning, and tests coding tools and deployments while ensuring compliance with clinical research regulations and quality standards.