Teams at Celerion

Build and administer EDC trials including eCRF design and EDC builds, program edit checks, create test data and environments, execute UAT coordination, program reports/listings with Veeva CDB, manage secure data imports, validate system upgrades, and maintain CDISC database standards.

Support development of bioanalytical scopes, budgets, and pricing; prepare proposals, RFQs, and contracts; manage project financials (forecasting, WIP, invoicing); maintain systems and templates; improve processes using Smartsheet, AI, and automation; coordinate cross-functionally to ensure accurate, compliant proposals and project financial alignment.

Build, configure and validate Veeva EDC/CDB clinical trial databases and eCRFs, program edit checks and reports, create test data, coordinate UAT and ensure secure data transfers and CDISC standards compliance.