Viedoc Database Developer

Viedoc Database Developer | Global CRO | UK or Europe | Permanent | We have an urgent requirement for a Viedoc Database Developer with a background in clinical data management. Interviews are taking place as soon as possible. This is a clinical trial database development role focused on building studies in Viedoc, programming edit checks and custom functions, and delivering work across several study timelines. Responsibilities:Build and maintain clinical trial databases using Viedoc Architect.Develop forms, matrices, edit checks, derivations, ALS and custom functions.Support UAT, validation documentation and change control in a GxP environment.Apply clinical data standards throughout database development. RequirementsAt least five years’ clinical database development experience, including hands-on Viedoc work on clinical trials.A background in clinical data management, with strong database build and programming experience.Strong Viedoc Architect skills and experience programming edit checks and custom functions.Working knowledge of CDISC, CDASH, 21 CFR Part 11 and ICH GCP.A degree in life sciences, computer science or a related field.The right to work in the UK or Europe. Experience developing a global standards library, working across different therapeutic areas and study phases, or supporting multiple sponsors within a CRO would be an advantage. If you have the relevant Viedoc experience, please share your CV or get in touch for a confidential discussion [email protected]