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4 Ways ClinEssentials Tools Can Benefit Your Company

4 Ways ClinEssentials Tools Can Benefit Your Company

by ClinEssentials Team | Jan 17, 2022 | Tools for Research Professionals, CROs & Sponsors

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...
7 Ways to Decrease CRC and CRA Turnover and Increase Efficiency

7 Ways to Decrease CRC and CRA Turnover and Increase Efficiency

by ClinEssentials Team | Jan 3, 2022 | CROs & Sponsors, Tools for Research Professionals

As a Sponsor, Clinical Research Organization (CRO) or Clinical Research Site, you want Clinical Research Associates (CRAs) and Clinical Research Coordinators (CRCs) who are master multi-taskers, efficient, and organized. However, due to high industry-wide turnover...
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 | Tools for Research Professionals, Clinical Research Associates, Tips for Research Professionals

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...
CRA Burnout and How to Avoid It

CRA Burnout and How to Avoid It

by ClinEssentials Team | Oct 25, 2021 | Clinical Research Careers, Clinical Research Associates, Tips for Research Professionals, Tools for Research Professionals

CRA Burnout. If you are in the clinical research industry, this is likely a phrase that you have heard or experienced. The reality is that CRA Burnout is becoming an increasingly bigger issue over time – for CRAs and their employers. Work performed by CRAs is...
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 | Tools for Research Professionals, Clinical Research Associates, Tips for Research Professionals

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...
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Recent Posts

  • The Most Common Pain Points Across Clinical Research Roles — and What to Do About Them
  • How to Build a Foundation for Aspiring and New Clinical Trial Managers
  • What I Wish I Knew Before Becoming a CTM
  • How to Break into Clinical Research in Five Steps (Even Without Experience)
  • What is the Difference Between a CRC and a CRA?

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REVOLUTIONIZING QUALITY & EFFICIENCY IN CLINICAL RESEARCH SM

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REVOLUTIONIZING QUALITY & EFFICIENCY
IN CLINICAL RESEARCH SM

ClinEssentials, LLC.  All rights reserved.
Terms of Service | Privacy Statement