Research Training Programme

An overview of the Research and Development department, facilities and processes for all new colleagues

R&D New Staff Induction

What happens to a research study after the end of trial declaration?

Archiving in Research

Establishing capacity and capability (C&C) is a very important step in setting up a research trial. Join this course to find out more about the behind the scenes of setting up a research study

Feasibility and Study Set-Up

Hand hygiene is only the beginning. This course covers the legal framework behind handling human tissue, equipment handling requirements and more

Handling Bodily Fluids

High quality documentation is vital to the healthy development of a research trial. Join this course to learn why.

High Quality Documentation

'Informed Consent' is a mandatory step in the design and delivery of a research trial. This course will explain why.

Informed Consent

What do you think counts as Intellectual Property? How many types of IP are there? Join this course for an exploration of IP in research and how this can benefit the healthcare system

Introduction to Intellectual Property

This course explores the trajectory of a research study from the idea stage to the moment when ethical approvals are in order

Leading Research (Pre/Post Award)

What does oversight of a research study truly mean? Who is responsible for what? This course is aimed at existing PIs and means to offer practical guidance and support in the performing of PI activities

Principal Investigator (PI) Oversight Masterclass

What is safety reporting and why should pharmacovigilance be practiced? How do they apply to a research study?

Safety Reporting (Pharmacovigilance)

What is the Investigator Site File (ISF)? How should this be managed and why is it important for the health cycle of a research study?

Site File Management