Why Clinical Trials Begin with a Project Kick-Off Meeting (KOM)
The Project Kick-Off Meeting is an essential one-time meeting during which core representatives from the Sponsor and CRO discuss study goals, timelines, and next steps for study activation. The KOM allows the team to meet one another and prepare for a successful trial start.
Conference Call Technology Tips for Clinical Trial Managers (CTMs)
To successfully get through your hours of conference calls, you need to be well-versed on all platforms, prepared with agendas and slide decks, and equipped with a backup plan. You can ensure this happens by being early for your meetings and having technology accessories readily available.
Work-Life Balance for Clinical Trial Managers
The achievement of work-life balance is critical to a Clinical Trial Manager’s ability to consistently deliver high-quality work.
What Does a Clinical Trial Manager Do?
Clinical Trial Managers are in high demand and their role is at the center of every clinical trial. But what do they actually do?
7 Steps to a Successful Research Study Transition
An effective study transition sets the Clinical Trial Manager or Clinical Research Associate up for success. Forgoing a study transition can lead to project delays and increased stress.
How to Plan a Productive Site Monitoring Visit
Planning for a clinical trial monitoring visit is the best way CRAs can ensure things run smoothly, efficiently, and effectively.
4 Ways ClinEssentials Tools Can Benefit Your Company
ClinEssentials Tools save time and increase efficiency in clinical research by streamlining communication.
7 Ways to Decrease CRC and CRA Turnover and Increase Efficiency
Retaining the best CRAs and CRCs has become a major challenge in the Clinical Research Industry, but there are ways to help reduce CRA turnover.
How to Develop an Efficient Visit Monitoring Process – and Close Action Items Quickly
Developing processes to increase efficiency for visit monitoring and closing action items will lead to more effective CRAs and Clinical Research Teams.
How To Create Efficiencies in Daily Clinical Trial Monitoring
There are opportunities for Clinical Research Associates to create efficiencies in daily monitoring that can lead to great job success for both experienced and new CRAs.
CRA Burnout and How to Avoid It
CRA Burnout is becoming an increasingly bigger issue over time. When Clinical Research Associates are able to achieve more of a work/life balance, they are able to deliver higher quality work.
6 Key Items to Look for When Monitoring an Informed Consent Form
CRAs are responsible for monitoring Informed Consent Forms for their clinical trials, and making sure the ICFs are completed correctly is very important.