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Viedoc Database Developer | Global CRO | UK & Europe | Contract | Urgent Requirement
We have an urgent requirement for a Viedoc Database Developer to support a clinical trial of medium complexity. Interviews are being arranged ASAP.
This is a hands-on database programming position, working as an individual contributor under a Data Management Lead.
You will have 4–6 years’ clinical database development experience and at least 4–5 Viedoc study builds personally completed, with the confidence to own a build from initial design through testing, release and ongoing changes.
Key responsibilities
* Design and build eCRFs in Viedoc Designer.
* Develop and test edit checks and derivations.
* Support UAT and maintain validation documentation.
* Implement mid-study and post-production changes.
* Deliver the database build against agreed study timelines.
Requirements
* 4–6 years’ total clinical database development experience within clinical trials.
* At least 4–5 Viedoc study builds completed directly.
* Solid experience across eCRF design, edit checks, derivations, UAT and database changes in Viedoc.
* Working knowledge of CDISC/CDASH, 21 CFR Part 11 and ICH GCP.
* Comfortable owning a build end to end under a Data Management Lead.
* The right to work in the UK or Europe.
* Viedoc Designer certification is preferred but not essential.
Practical Viedoc build experience is the core requirement.
Please send your CV to , including your availability and rate expectations, or message me directly for a confidential discussion.
We also support other opportunities across pharmaceutical, biotechnology and CRO organisations throughout Europe.