Training designed for clinical research professionals
EUCRIT training is built to help professionals understand Good Clinical Practice, strengthen operational competence and apply clinical research principles in real site environments.
Our training includes a clinical research and GCP essentials course, an ICH E6(R3) GCP certification, a practical soft skills course for site staff, a site-specific GCP practical training session and a downloadable operational manual for day-to-day reference.
Introduction to ICH E6(R3) GCP
A concise, accessible introduction to clinical trials and Good Clinical Practice under the ICH E6(R3) guidelines. Designed for those who want to understand the foundations before moving to full certification, or for anyone looking for a clear entry point into clinical research.
ICH GCP E6(R3) — Investigator Site Personnel
This course provides a thorough and structured overview of the Good Clinical Practice guidelines relevant to investigator site personnel. It is fully self-paced and accessible across devices.
Each of the 20 lessons includes a video lecture with subtitles, followed by a visual summary designed to consolidate the key concepts covered. A dedicated glossary section introduces and explains the most relevant terminology.
Upon passing a final assessment, the course awards a CPD accredited certificate. The course also meets the Minimum Criteria identified by TransCelerate BioPharma for mutual recognition of GCP training among trial sponsors, meaning your certificate will be recognised across sponsors and CROs worldwide.
Site Staff Soft Skills Training
Clinical research is not only about protocols and compliance. It is about communication, organisation, and the daily decisions that keep a study on track. This course builds the practical professional skills that make site staff more effective from managing priorities to working with sponsors and caring for participants.
Site-specific GCP Practical Training (2 hours)
A live, interactive training session designed around the specific needs of the investigator site. Delivered via video call by an expert trainer, this course translates core GCP principles into practical guidance for site-level activities.
Rather than a standardised format, the session is tailored to the site's profile and team, allowing direct interaction with the trainer, real-time questions, and discussion of practical scenarios relevant to day-to-day site conduct.
Investigator Site Personnel Operational Manual
The Investigator Site Personnel Operational Manual is a comprehensive reference resource covering all the key aspects of clinical trial conduct at the site level. Grounded in the ICH E6(R3) GCP guidelines, it goes beyond the regulation to explain the operational rationale behind each requirement giving site staff the deeper understanding they need to work with confidence, not just compliance.
Explore which EUCRIT plan includes the training you need.
EUCRIT training offerings are integrated into membership plans for professionals and investigator sites. Review the available plans to choose the level of access that fits your needs.