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7 Steps to a Successful Research Study Transition

7 Steps to a Successful Research Study Transition

by ClinEssentials Team | Jul 6, 2022 | CRA/CRC Tools

Inheriting a study from an outgoing Clinical Research Associate (CRA) or Clinical Trial Manager (CTM) happens frequently in the Clinical Research industry. If you have been involved with a study transition, you know that it can be a challenge for the incoming team...
4 Ways ClinEssentials Tools Can Benefit Your Company

4 Ways ClinEssentials Tools Can Benefit Your Company

by ClinEssentials Team | Jan 17, 2022 | CRA/CRC Tools

ClinEssentials knows how frustrating it can be for each hiccup to result in much longer trial times and budget overspend. That’s why we develop products that save CRAs time by streamlining communication with their clinical research site teams. These are 4 proven ways...
How to Develop an Efficient Visit Monitoring Process – and Close Action Items Quickly

How to Develop an Efficient Visit Monitoring Process – and Close Action Items Quickly

by ClinEssentials Team | Nov 22, 2021 | CRA/CRC Tools

Clinical Research Associates (CRAs) have a plethora of responsibilities for the clinical trials they manage. One of their main responsibilities is the management of action items. CRAs are accountable for documenting action items, notifying the clinical research team...
How To Create Efficiencies in Daily Clinical Trial Monitoring

How To Create Efficiencies in Daily Clinical Trial Monitoring

by ClinEssentials Team | Nov 8, 2021 | CRA/CRC Tools

Clinical Research Associates (CRAs) are extremely important members of Clinical Research Teams, and play a crucial role with clinical trial oversight. A CRA acts as a liaison between a research study Sponsor or Clinical Research Organization (CRO) and the clinic where...
6 Key Items to Look for When Monitoring an Informed Consent Form

6 Key Items to Look for When Monitoring an Informed Consent Form

by ClinEssentials Team | Oct 12, 2021 | CRA/CRC Tools

CRAs are responsible for monitoring each Informed Consent Form (ICF) for their clinical trials. Since they involve the consent of trial participants, making sure the ICFs are completed correctly and entirely is very important. Paying attention to the details will help...
5 Essential Items for a Clinical Research Associate’s Work Bag

5 Essential Items for a Clinical Research Associate’s Work Bag

by ClinEssentials Team | Oct 12, 2021 | CRA/CRC Tools

Have you found yourself at a site visit, digging through all of the important things in your work bag but not able to find the one thing that you really need? We’ve been there. Do you spend time preparing and organizing your work bag before traveling to various trial...
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