New Free Resources: Trial-Level Oversight Metrics, QCs, and Our Methodology at a Glance

|Anders Mortin
New Free Resources: Trial-Level Oversight Metrics, QCs, and Our Methodology at a Glance
Free Resources · TriTiCon Knowledge World

New Free Resources: Trial-Level Oversight Metrics, QCs, and Our Methodology at a Glance

From our training module on Oversight in Clinical Development

Before heading into the weekend, we're publishing another round of free resources from our training module on Oversight in Clinical Development. These materials are designed to be practical, adaptable, and immediately useful for sponsors working with vendors across the clinical development lifecycle.

What's new

Three new documents are now available for download — two companion catalogues covering oversight across the key disciplines of clinical trial delivery, and a short methodology overview that distills our approach into a format you can read in minutes.

Two oversight catalogues

Together, the two catalogues provide a comprehensive view of what to measure, monitor, and approve when overseeing vendor performance on a clinical trial. Both span the core disciplines involved in trial delivery:

  • Clinical Data Management
  • Statistical Programming
  • Biostatistics
  • Safety Handling
  • Trial Management
  • Site Management
Catalogue 1
Trial-Level Oversight Metrics and Approvals
Suggested KPIs, quality indicators, and approval checkpoints for monitoring vendor performance within an individual clinical trial. Structured for review at trial-level oversight meetings and designed to feed into portfolio-level reporting.
Catalogue 2
Oversight QCs and Spot Checks
Concrete quality control activities and targeted spot-check procedures that sponsors can apply across the same disciplines — a practical companion to the metrics catalogue.

Both documents are intended as starting points. Download, adjust, and use — adapt them to your organisation's structure and risk profile, and put them to work right away.

Oversight – TriTiCon Methodology at a Glance

The methodology in 2.5 pages and two key slides

We've also published a short overview that distills the principles of the oversight methodology we teach into 2.5 pages and two key slides. If you want a fast introduction to how we think about vendor oversight — the philosophy, the building blocks, and how the pieces fit together — this is the place to start. Have a look!

Why we're sharing these

Effective oversight is one of the areas where sponsors most often tell us they want clearer structure and more practical tools. By making these catalogues and the methodology overview freely available, we hope to give teams a useful baseline they can build on — whether you are establishing oversight processes for the first time or refining an existing framework.

Download the resources

Free to use. Adapt them to your own setup and put them to work.

Get the Resources →

Questions or feedback? We'd be glad to hear from you.

Anders Mortin

Clinical Data Management Expert

TriTiCon delivers clinical data management training based on extensive hands-on experience from real clinical trials across sponsors, CROs, and life sciences organizations. The training is developed by industry professionals who work directly with clinical data, systems, documentation, and cross-functional trial teams.

30+
Years Experience
50+
Clinical Trials