This webinar was presented live on Wednesday, March 13, 2019. Click below to watch it on demand.
What do you do when your clinical study seems to have gone “off the rails” due to inexperienced staff, high turnover, ill-prepared monitors, a poorly written protocol or a general lack of resources?
With all of the moving parts involved in running a clinical trial, even the most seasoned researchers will experience issues. So how do you pick up the pieces and salvage the study? Using real world experiences as the backdrop, this webinar will explore why this happens and provide recommendations for how to tackle the issues. Presented in a discussion format, two speakers who have been involved with many study rescue efforts will give you practical solutions that can guide you as you work toward getting your study back on track.
By attending this webinar you will be able to:
- Identify at least three root causes that can lead to a non-compliant study;
- Discuss at least three techniques that can be used to help bring a study into compliance;
- Discuss the importance of establishing a clear plan, defining roles and responsibilities and measuring progress throughout a clinical study rescue effort.
Featured Speakers:
Sandra Maddock
President/CEO
IMARC Research
Brandy Chittester
Chief of Clinical Operations
IMARC Research
Danielle Kirsh
Assistant Editor
Medical Design & Outsourcing
Sponsored By: