EU EDITION - SPONSOR RESPONSIBILITIES IN CLINICAL TRIALS MASTERCLASS

02-03 SEPTEMBER, 2025

Working knowledge of sponsor responsibilities for clinical trials

SPONSOR RESPONSIBILITIES IN CLINICAL TRIALS MASTERCLASS - EU EDITION

ONLINE MASTERCLASS | 02-03 SEPTEMBER, 2025

Starting time: BST 13:00 p.m.

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Key Takeaways

Elements of the sponsor Quality Management System

Vendor selection, management and oversight

Contracts and contract management

Risk assessment and management processes

masterclass in pharma

Overview

This course is designed to provide an up to date working knowledge of Sponsor Responsibilities for Clinical Trials along with practical guidance on oversight of clinical trial sites and outsourced activities.

The course will cover Sponsor requirements in the latest Good Clinical Practice guidance documents and some of the main differences in legal obligations in specific geographical regions (for example, the USA and the EU).

The course will be interactive with opportunity for questions and practical discussion of case studies and example inspection findings.

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MEET THE TRAINER

Jo Burmester

Clinical Research Trainer
Logic Squared Ltd trading as JoBurmester.com

Jo Burmester is a very experienced Clinical Research Training Consultant who has provided GCP expertise for many years. She works with a wide range of clients and her passion is making GCP interesting and relevant.

Jo is a pharmacology graduate and began her career in clinical research in 1987. She started out as a CRA and then moved into a training role. She was a founding director of PharmaSchool, a specialist clinical research training company, for 14 years, and then in October 2018 she moved on from there to work independently.

She holds a Certificate in Training and Development from the Chartered Institute of Personnel and Development, and was a Module Leader on the Clinical Research MSc programme run at Liverpool John Moores University. She is the author of a book on Continuing Professional Development and regularly chairs and presents at international clinical research conferences.

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Reasons to attend a masterclass

Practical knowledge

Venture into undiscovered territories and gain inspiration through collaboration

Interactivity

Boost your professional skills by directly engaging with domain experts

World-class trainers

Gain value and learn from the best instructors

Networking

Build a top-notch community and advance your career

Who should attend?

-Medical monitors
-Medical directors
-Clinical trial manager
-Clinical scientists
-Clinical researchers
-Clinical operations managers/leaders/directors/heads
-Clinical project managers
-Clinical contracts managers