Remote Monitoring and Future Opportunities during COVID-19 and Beyond – Webinar
Book a session
| Date | Product | Location | Price | |
|---|---|---|---|---|
| No sessions are planned at this time, however if you are interested in taking this course click here | ||||
| If you would like to have this course as an in-house session click here | ||||
About this course
Reasons to attend
This interactive webinar is developed to help you understand the different impacts caused by COVID-19 on Clinical Trials, as well as potential solutions at both the operational level and the future strategic direction by providing you with a detailed description of what is remote monitoring and what it is not.What's included?
- Documents and materials related to this course are included
- Globally recognised certificates awarded after test completion
Course Description
COVID-19 has had a major disruptive impact on Clinical Trials. This 2-hour highly interactive webinar is intended to provide you with an overview of the impact COVID-19 has on clinical trial management and how you can increase remote-monitoring to minimize the impact.We will also delve into the pros and cons of remote monitoring and provide you with tools to start remote monitoring, even if you have never done so before. As the future of performing clinical trials “as usual” has been dramatically altered due to COVID-19, we will share with you the virtues of remote monitoring, decentralized studies or virtual studies and remote patient data collection and, collectively, peer into the future.Be prepared to share any specific questions you may have related to your own circumstances and benefit from the collective wisdom of the experienced facilitator as well as the other attendees.Programme highlight
- How to Minimize the Impact of COVID-19 on your Clinical Trial
- How and where to start remote monitoring if never done before
- How to be sure that remotely-monitored data are reliable?
- Pros and Cons of remote monitoring
- Possible techniques to implement NOW for your ongoing clinical trials
- Are physical site monitoring visits a thing of the past?
Learning objectives
- Obtain a clear understanding of the challenges to clinical trials today due to COVID-19 and how to minimize the impact on your clinical trials
- Learn about potential solutions that can be implemented now to keep your ongoing trail as “on-track” as possible
- In depth review of Remote-Based Monitoring activities – what it is and what it is not - and why it is so important moving forward
- Recognize the needs of the patient by implementing a “patient first” attitude in your clinical trials
- Acquire ideas for potential long-term opportunities and future design of clinical trials that come from the COVID-19 impact
Who should attend
Clinical Project Managers, Clinical Research Associates and Clinical Trial Assistants.Previous knowledge of the basics of clinical research, Good Clinical Practice and ICH Guidelines is expected.
Competencies
This course covers competencies that are part of the ECCRT Competency Framework
- Scientific Concepts & Research Design ()
- Ethical & Participants Safety Considerations ()
- Investigational Product Development and Regulation ()
- Clinical Studies Operations (GCPs or ISO 14155) ()
- Study and Site Management ()
- Data Management and Informatics ()
- Leadership and Professionalism ()
- Communication ()
- Teamwork ()
- Business acumen ()
Trainers
Dr. Paula Hemdal
TrainerTestimonials
- This webinar helped me to better understand on how to manage communication and visits with/at sites. The course was a positive experience in general in terms of guidance and tools to support monitors in such public health crisis.