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...
by ClinEssentials Team | Feb 28, 2022 | CRA/CRC Tools
Many Clinical Research Associates are unprepared for their clinical trial monitoring visits, which is an important part of their role. It is understandable – CRAs are busy and it can be hard to find time for planning where there are so many other tasks to...
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...
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...
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...
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...
