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Regulating the Workload of Your Clinical Research 
Coordinator (CRC) 
A CRC (clinical research coordinator) is one of the most important people regarding 
clinical trials. He/she is the person who’s in charge of conducting the clinical trial, 
under the guidance of the PI (principal investigator). As the people responsible for 
coordinating all the activities on site, CRCs can sometimes carry a huge workload. 
This can quickly become a big problem not only for the CRC but also for everyone 
else involved in the study.  
 
Determining the right workload for your CRC is one of the most important actions 
that you (as a site owner or PI) should take. Ideally, a CRC should work 4 to 6 
effective hours per day. However, you will notice that there will be periods of time 
when the CRC has to work more than 8 hours but also periods when he/she will be 
free most of the days. In this article, we’ll help you find the right balance so that 
your CRC isn’t too overworked or underworked.  
 
 
The CRC workload depends on many variable factors: 
 
- The complexity of the study​ - How complicated a study is can be one of the 
greatest factors when you’re determining CRC workload. Some studies are 
really simple while others can be extremely complex. Patient visits in simpler 
studies can last only for some minutes, while in more complicated studies 
these visits can last over 5 hours. These are all important factors that should 
be taken into consideration when you’re looking at your CRC’s workload. 
- The frequency of patient visits​ - Do the patients only come once? Do they 
have to come back every 30 days? Or once a week? Or every second day? 
These are all questions that determine the workload of the CRC. 
- The number of enrolled patients​ - Even if a site has various open studies, 
usually they don’t manage to find the targeted number of enrolled patients 
for all of them. Normally, sites would only have one or two active studies 
which are active and for which they actually managed to enroll the desired 
number of patients. The number of active studies, as well as the number of 
enrolled patients in each study, are two important factors that can show you 
the CRC workload.  
 
 
A simple example of CRC workload (to simplify your calculation 
process): 
 
1st case scenario: Daily Patient Visits 
 
Let’s say that one typical patient visit lasts for 1 hour (although some might be 
much more). After every patient visit, the CRC will need approximately 3 more 
hours to gather and enter all the data. So this means that the CRC will have 4 to 5 
hours of actual work in a day. A normal working day is usually 8 hours. This leaves 
the CRC with enough time to have a lunch break, coffee break, as well as to finish 
some smaller daily tasks or talk to colleagues. In this case, the CRC isn’t overworked 
but probably won’t have much time to handle and coordinate other site activities. 
 
2nd case scenario: Patient Visits Every Second Day 
 
This second scenario is much more likely to happen at most sites. The CRC will 
normally not have patient visits every day (except if the number of participants is 
huge), but maybe every second day. This gives the CRC many free days which 
he/she can use to coordinate other site activities.  
 
3rd case scenario: Multiple Short Patient Visits per Day 
 
In this last case, patient visits might last 10 or 15 minutes (again, depending on the 
type of study), so the coordinator might have multiple patient visits per day. In this 
case, when the CRC receives two or three patients per day, he won’t have time to do 
other site activities as well (since he will also have to take care of all the data after 
patients leave).  
 
In all of these above cases, CRCs aren’t overworked. However, if you give them 
additional work apart from the above-mentioned, then this will be considered as a 
big workload. Try to follow the workload (daily activities) of your CRC for a period of 
time in order to determine if he/she is overworked or underworked. Knowing this 
will help you take the necessary steps to fix it. If the CRC is overworked, you can 
either hire someone as help or maybe give some of his tasks to another staff 
member.  
 
 
Working in Compliance 
 
Another thing that has many site owners worried is if the CRC is working in 
compliance and by the law. If there’s something wrong with the way a site is 
operating, your monitors will notify you immediately on their next visit. The only 3 
things that CRCs and other site staff need to respect are to follow:  
- GCP (Good Clinical Practice); 
- SOP (Standard Operating Procedures); and 
- The study protocol; 
 
If your CRC follows these 3 practices, then there’s really nothing to worry about. In 
any case, even if the quality of work of your CRC is not good, your monitors will let 
you know on their next visit (they will usually visit your site every 6 weeks).  
 
Another thing you can do if you wish to further ensure the quality of your CRC’s 
work is put in place a QA system (quality assurance). The people who are 
responsible for QA will basically double-check the work of your CRC after every 
patient visit in order to make sure that everything is done correctly. Doing this can 
greatly improve your CRC’s work and all the operations on site.  
 
 
Conclusion 
 
To sum up, the workload of CRCs can greatly vary from site to site. This depends on 
many factors such as the nature of the study, the number of enrolled patients, the 
number of active studies, the longevity of patient visits, etc. In any case, there can 
be periods of time when the CRC is overworked, but there will also be periods when 
he/she is underworked. So, finally, you as a site owner should follow the CRC’s 
workload and make sure that there’s a balance. A coordinator who’s constantly 
overworked won’t be able to perform well.  
 
 
 
Visit ​https://trialjoin.com/research-resources/​ for more articles
Or Call
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