Principal investigators
Study oversight, eligibility, safety reporting, and protocol responsibilities.
Turn every study protocol into role-based training.
Upload the approved protocol and study manuals, then personalize every lesson by site role, assessed gaps, and progress. Keep dated completion records in one place.
Over 1 million learners have trained on Kampster across businesses, governments, and universities.
Every role learns the protocol differently.
Sponsors, CROs, and site networks keep one approved study standard across every site. Each person gets lessons matched to their responsibilities, current understanding, and progress.
Principal investigator
Study coordinator
Pharmacy & lab
Data team
Study protocol
Clinical research coordinators
Visits, recruitment, documentation, timelines, and the procedures deviations come from.
Pharmacy and laboratory teams
Product handling, sample workflows, storage conditions, and role-specific procedures.
Data and supporting teams
Data collection, system workflows, reporting requirements, and deadlines.
From approved documents to prepared study teams.
A protocol explains what must happen. Kampster shows that every person understood the part they are responsible for.
Build from the approved sources.
Add the protocol, Investigator’s Brochure, laboratory manuals, and pharmacy guidance. Kampster AI structures them; your clinical team approves what publishes.
Explore the course creatorCheck that each role understood.
Assessments show what investigators, coordinators, pharmacy, laboratory, and data teams took from the material.
Explore assessmentsKeep the training record.
Retain dated completion evidence by study, site, role, and person, ready before the monitoring visit.
Explore skill intelligence
Keep training aligned as the study changes.
When the protocol is amended, update the affected learning. Kampster assigns the changed content to the roles it touches and keeps each person’s remaining gaps in view.
Update the affected lessons
Keep the learning material aligned with the approved protocol and its supporting documents.
Retrain the relevant roles
Send follow-up training to the people and responsibilities the change actually touches.
Keep a dated record
Hold completion evidence against the study materials and version it belongs to.
See which sites are ready.
Monitor training across the study and find missing roles, incomplete learning, and knowledge gaps while there is still time to act.
Completion by site
Progress across hospitals, countries, and study locations, in one view.
Coverage by role
Confirmation that every required role has received the training it needs.
Comprehension by module
The procedures and requirements that need explaining a second time.
Documented completion
Assessment results, timestamps, and role-specific certificates kept together.
Your company’s knowledge stays your company’s.
Kampster is built to SOC 2 controls and follows ISO 27001 practices. Your content is never used to train anyone’s model.
- GDPR-aligned
- Built to SOC 2 controls
- ISO 27001 practices
- Zero Data Retention
Developed in official partnership with Harmony Trials. Kampster provides the learning technology; Harmony Trials contributes clinical operations, regulatory, and site-management expertise.
Explore more use cases.
Common questions.
Upload study protocols, Investigator’s Brochures, laboratory and pharmacy manuals, safety guidance, slide decks, and other approved training materials. We define the exact source set with your team during setup.
Kampster AI structures the approved source material into proposed modules, role-based paths, and assessments. Your study team reviews and approves everything before it is assigned.
Yes. Common requirements remain consistent. Each person receives lessons based on their role and assessed gaps, and the path adjusts as they progress.
The affected learning can be updated and assigned as focused retraining. New completion records remain connected to the relevant study materials and protocol version.
Teams can track completion, assessment results, timestamps, certificates, and progress by study, site, role, or individual.
No. Kampster adds structured, protocol-specific learning alongside GCP, system, laboratory, pharmacy, and procedural training. It supports your training process but does not by itself guarantee regulatory compliance.
Prepare every sitetoday.
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Start with one study. Expand when the workflow is proven.