Your database is your clinical trial. It's how your study is represented to the FDA — no matter how well it ran at the bedside.
WST Consultancy is a boutique, founder-led clinical data management firm that works as an extension of biotech and pharma teams, from first record to database lock.

The case we make to sponsors is simple. For the clinical side of a trial, a large CRO earns its keep. For data management, it quietly costs you more than it should — in money, in months, and in the capability you never build. Bundled DM is priced at team rates for a team that rarely materialises, run through a slow review loop that adds a month at a time; when the contract ends you keep the deliverables but none of the systems, SOPs, or know-how. A single genuinely technical data manager — one who reads the monitoring and statistical plans and programs the database — replaces that whole chain.
We work inside your systems, write your SOPs, and build your documents with you. You come out faster, cheaper, and with a data management function you actually own.

What we own, end to end: data management strategy, EDC and database build, edit checks and validation, query management, risk-based and statistical monitoring, MedDRA/WHODrug coding and CDISC (SDTM/ADaM), SAS programming, dashboards and reporting, SAE and external reconciliation, and database lock.
Fluent in the platforms your trial already runs on — Medidata Rave, Veeva Vault CDMS, Oracle InForm, Medrio, TrialMaster — and built to 21 CFR Part 11, ICH-GCP, CDISC and GCDMP from day one.
Ways to work: full-study data management, embedded/fractional support, or rescue and remediation.
Chicago, IL. Let's talk about your study — hello@wstconsultingagency.com


WST Consulting

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WST Consulting

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