Learning Management

Take Control of Clinical Trial Training

Give your sites the courses and credits they need to succeed with the Learning Management module of the Investigator Site Portal.

Site attrition rates are soaring

The Great Resignation has hit clinical research sites hard. With fewer and less experienced site staff available to run your trials, your training curriculum needs to be more effective than ever. But asking site staff to take redundant GCP and protocol training is counterproductive and frustrating.

Without a new approach to learning management across your clinical programs, training compliance will decline while protocol deviations climb, putting your trials at risk.

Challenges with general-purpose learning management systems

You may have tried to eliminate paper/email-based site-training with a general-purpose or corporate learning management system (LMS). But it doesn’t have the features you need to distribute courses and track compliance through the complexity of site roles and regulatory inspections.

What if you could have an enterprise-level LMS that was built specifically for training sites across all your protocols, therapeutic areas, and geographies - and gave you all the features you need for complete oversight plus high site satisfaction? Could your studies start-up faster and run more smoothly?

Cross-Trial Training from IQVIA Technologies

The LMS module of the IQVIA Investigator Site Portal gives you a centralized solution for distributing training courses to investigators and site staff that are studying your compounds around the world.

A global catalog of courseware and powerful workflow enables study teams and training professionals to push trainings based on roles, countries, and studies

Cross-trial logic ensures that site personnel automatically receive credit for courses already completed

Dashboards give instant insight into compliance, so you can say good-bye to manual trackers

Digitized Training Journey

A win/win for investigator and sponsor value

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