As CPM you'll be responsible for leading study teams in the management of budgets, timelines and study conduct. You'll oversee the quality and scientific integrity of the trial to ensure patient safety, data credibility and compliance within governing rules and regulations.
I think one of the most important features of the course was getting to learn from experts in the field. Even this anecdotal information taught me a lot about the best standards and how I need to conduct myself as an efficient CPM.
Sat 09th – 24th Sept 2023
Sat18th Nov – 03rd Dec 2023
Sat 10th – 25th Feb 2023
Mon 16th – 18th Oct 2023
Mon 22nd – 24th Jan 2024
Sat10th – 25th Feb 2023
As a CPM you'll require:
If you are looking to enter the field of clinical research, this CPD accredited 3-day course is for you. It will provide you with a comprehensive insight into trial objectives and create an effective project plan. Considerable attention is given to the critical stages of planning, setting up a clinical trial and setting clear and realistic milestones.
This course examines key trial stages and guides you along with the key activities you will need to carry out at each stage.You'll have hands-on practice using project management tools that you would use in the role as well as learning vital techniques for effective project management. All your interactive learning will be within the context of the regulations and rules governing clinical trials with activities being based on real case studies and scenarios.
This module will look at:
You will also be guided through some real-life practical training that you will experience on the job.
Very good course. The course was very useful with a vast amount of information that has been simplified in a good way. Enjoyed the workshops.
If you are a Clinical Research Associate who is transitioning into your first project management role, or an Associate CPM who has been promoted; this modular training is specifically designed for you.
You may be a CPM going from a CRO to a pharmaceutical CPM role, or a regional Clinical Trial Manager who is transitioning to a global CPM. This is an excellent starter course, that will equip you with the skills to conduct your role to manage the budgets, milestones, timelines, and quality of the clinical trials that you lead.
With a BSc in Chemistry, PhD in Organic Chemistry and a Postdoctoral Research Fellowship at the Institute of Biotechnology at Cambridge University, Dr Lia Hunter's career has spanned 30 years in clinical research. Founder and Director of both CGX Training and Clinnovate Ltd, Dr Hunter has worked for and with world-renowned pharmaceutical organisations, including Pfizer, Biogen, Takeda and AbbVie.
Donna-Marie Donalds’ career has spanned more than 20 years. Starting as a CRA for the Thrombosis Research Institute in 2001, she has since worked with the likes of Johnson & Johnson, Covance and Sanofi-Aventis. She is currently the Managing Director of QC Monitoring Solutions while freelancing as a clinical research consultant. Donna-Marie is also Head of Training and the innovative course creator at CGX Training.
As a clinical project manager, you're in charge of a number of clinical trials, at every stage of the process, across multiple sites.
The responsibility can feel overwhelming, so here at CGX Training we have specifically designed a hands-on course full of real-world scenarios so you have the confidence and practical knowledge to manage situations efficiently without the guesswork.
Plus, you'll also be carefully guided through the job application process, with insider tips on how to create a standout CV and nail that interview.