Clinical Research Courses for Top Jobs
Including MHRA-aligned certification โ recognised across the UK and globally
Showing 10 of 10 courses
Good Clinical Practice (GCP)
Clinical Trial in the UK: Start-up to Closure
End-to-end guide to running clinical trials in the UK under MHRA regulations
Good Clinical Practice (GCP)
ICH GCP E6(R3) Fundamentals for UK Clinical Research
Master GCP compliance with a focus on MHRA and UK regulatory requirements
Good Clinical Practice (GCP)
Clinical Research Associate (CRA) Foundation
Step into the role of a CRA with this role-specific UK training programme
Pharmacovigilance & Drug Safety
Introduction to Pharmacovigilance
Drug safety fundamentals for the UK and global clinical research context
Pharmacovigilance & Drug Safety
Adverse Event Reporting: MHRA & EMA Requirements
Master SAE and SUSAR reporting timelines for UK and EU trials
Clinical Data Management
Clinical Data Management Principles
CDISC standards, EDC systems, and data quality in UK clinical trials
Regulatory Affairs
UK Post-Brexit Regulatory Landscape
Navigating MHRA regulations after the UK's departure from the EU
Regulatory Affairs
Clinical Trial Authorisation (CTA) Process
Step-by-step guide to submitting CTAs through IRAS to the MHRA
Investigator & Site Training
Principal Investigator Responsibilities
Legal, ethical and operational duties of the PI under GCP and UK law
Investigator & Site Training
Protocol Deviation Management
Identifying, classifying, reporting and preventing protocol deviations