Viedoc Database Developer

Location: UK or Europe
Employment: 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.

Requirements

• At 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 send me your CV or get in touch for a confidential discussion.