Sponsor Responsibilities in Clinical Trials MasterClass - US edition

18-19 March, 2025

Inspection readiness

18-19 March, 2025, Virtual

Time Zone: Eastern Daylight Time (EDT) - UTC - 04:00

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Key learnings

Knowledge

Working knowledge of sponsor responsibilities for clinical trials

QMS

Elements of the sponsor Quality Management System

Vendor selection

Vendor selection, management and oversight

Contracts

Contracts and contract management

Risk assessment

Risk assessment and management processes

Oversight

Maintaining, documenting and demonstrating oversight

Trusted by over 17,000 delegates across leading companies

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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 opportunities for questions and practical discussion of case studies and example inspection findings.

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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 RECOMMENDATION

Who should attend?

Medical Monitor
Medical Director
Clinical Trial Manager
Clinical Scientist
Clinical Researcher
Clinical Operations Manager
Clinical Operations Leader
Director/Head of Clinical Operations
Clinical Project Manager
Clinical Contracts Manager

Ticket options for you

Full event
pass

Team participation?

*minimum of 10 participants

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Testimonial

Our success stories

"High attention to detail in course content and very well delivered"

Simon Halsey

Product Development Manager
Essentra Packaging
United Kingdom

Our success stories

"Very good training led by two knowledgeable and open experts. Excellent insight given on many complex topics. Interactive and highly useful"

Aurelie Vivicorsi

USP PD Team Manager
Celonic AG
Switzerland

Our success stories

"Great course, impressed with the knowledge of the trainers and ability to answer wide variety of questions!"

Emilia Szwej

Manager, Senior Investigator
MT Sword Laboratories (BMS)
Germany

About GLC

Global Leadership Conferences began as an ambitious dream by three founders ten years ago. Today its an international series of interactive events, exploring the hottest topics in critical fields. Each year, thousands of professionals join us to challenge the status quo and learn innovative ways to create new solutions in Finance, Pharmaceutical, HR, Health & Safety, and Energy.

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