Freelance data management focused on clean data, regulatory compliance and smooth trial operations — from protocol to the first eCRF draft and to final data handover.

Benno Jürgen Antoni
Senior Clinical Data Management Consultant
From protocol to the first eCRF draft and to final data handover —
tailored clinical data management for every phase.
End-to-end data management for clinical trials — from study start-up to database lock, focused on quality, compliance and on-time delivery.
User-friendly eCRF design in leading EDC systems, including logic checks, edit checks and a clean data structure.
Programming and review of validation rules. Early detection of inconsistencies, implausible values and missing data.
Fast, precise and communicative query handling. Fewer follow-ups, cleaner data and happier sites.
Work aligned with ICH-GCP, GxP, 21 CFR Part 11 and ALCOA+ principles. Documented, traceable and audit-ready.
Custom scripts, macros, data extracts and reporting solutions to automate workflows and improve data quality across clinical systems.
A transparent process, clear communication and no surprises —
that is how we deliver reliable data quality.
We clarify study objectives, system landscape, timelines and your specific data quality requirements.
eCRF design, data validation, workflows and the monitoring plan are tailored to your study.
Ongoing query management, data review, reconciliation and close alignment with your clinical study team.
Clean file preparation, database lock, archiving and handover-ready documentation for your submission.
Let's have a short call about how I can support your clinical data management — no obligation, project-based.
Pricing tailored to your study
Rates are based on project scope, study phase, complexity and required level of support.