Difference between revisions of "The clinical research associate or CRA will review and verify documents"
Hwangmarcus4 (talk | contribs) m |
m |
||
| Line 1: | Line 1: | ||
| − | The clinical research associate or CRA will review and verify documents from multiple sites conducting the same trial and do multiple visits to ensure quality and ethical conduct of the clinical trial. Having [https://ccrps.org/clinical-research-blog/cra-training | + | The clinical research associate or CRA will review and verify documents from multiple sites conducting the same trial and do multiple visits to ensure quality and ethical conduct of the clinical trial. Having [https://ccrps.org/clinical-research-blog/cra-training clinical research associate training] through CCRPS’s accredited Advanced Clinical Research Associate Certification course can help professionals 1) get promoted 2) get a raise 3) improve efficiency 4) get hired as a Clinical Research Associate. |
Latest revision as of 19:15, 21 April 2021
The clinical research associate or CRA will review and verify documents from multiple sites conducting the same trial and do multiple visits to ensure quality and ethical conduct of the clinical trial. Having clinical research associate training through CCRPS’s accredited Advanced Clinical Research Associate Certification course can help professionals 1) get promoted 2) get a raise 3) improve efficiency 4) get hired as a Clinical Research Associate.
