Analyzing the Data Monitoring Essay

Open, View, and/or
Download this Document

Total Length: 756 words ( 3 double-spaced pages)

Total Sources: 2

Page 1 of 3

Monitoring

Why is it important for the CRA to understand the data management and statistical analysis plans? What exceptions might there be?

The clinical research associate (CRA) has the main role and responsibility of carefully selecting fitting investigators, instigates and monitors the clinical trials at the different sites and, monitors the advancement of the study up until completion. In addition, the CRAs are also dispensed the accountability and obligation of thoroughly and effectually making groundwork for checking visits and initiate data evaluation and appraisal between visits. The clinical research associates have the liability for making sure that site visits are assured to be devoted and operational. It is imperative for the CRA to understand the data management and statistical analysis plans. This is because if the data entry clerk is not able to understand a field, or if the data appears to be contradictory or evidently improper, a report is directed to the CRA and a query is directed to the site to shed light on or rectify the data entry field being taken into consideration. Therefore, a lack of understanding implies that the CRA will not able to make corrections or rectifications of any problem (Mitchel et al., 2005).

Stuck Writing Your "Analyzing the Data Monitoring" Essay?

View All Our Example Analyzing the Data Monitoring Essay

Have A Custom Example Essay Written



It is imperative to point out that gathering data for the subjects or participants is not an everyday task or responsibility of the principal investigator. In essence, this is more often than not the accountability and task handed out to the clinical research associate (CRA). However, at times, there may perhaps exist some exceptions to this case. This encompasses a number of clinical trials. This is in the case where the final and ultimate accountability with respect to the gathering of data need to shift to the principal investigator. Most of all, however, the clinical research associate ought to be familiar with the data gathering protocol as well as advancement and progress (Clinical Tools, 2012). More so, it is imperative for the CRA to understand the plans being taken into consideration in data management. To be more specific, the responsibility and undertaking of data entry as well as the modification of data that is encompassed in data management are apportioned to the clinical research associate (CRA). The inference of this is that in order for the CRA to handle this responsibility, he or she ought to be well cognizant with statistical analysis plans and data management (Medidata, 2013).….....

Show More ⇣

     Open the full completed essay and source list


OR

     Order a one-of-a-kind custom essay on this topic


sample essay writing service

Cite This Resource:

Latest APA Format (6th edition)

Copy Reference
"Analyzing The Data Monitoring" (2016, January 13) Retrieved June 5, 2026, from
https://www.aceyourpaper.com/essays/analyzing-data-monitoring-2157830

Latest MLA Format (8th edition)

Copy Reference
"Analyzing The Data Monitoring" 13 January 2016. Web.5 June. 2026. <
https://www.aceyourpaper.com/essays/analyzing-data-monitoring-2157830>

Latest Chicago Format (16th edition)

Copy Reference
"Analyzing The Data Monitoring", 13 January 2016, Accessed.5 June. 2026,
https://www.aceyourpaper.com/essays/analyzing-data-monitoring-2157830
   

Open, View, and/or
Download this Document
order custom essay example