Difference between revisions of "1.5.2.5 Research team"

From EQIPD
Jump to: navigation, search
Line 1: Line 1:
 
== ​​​​A. Background & Definitions ==
 
== ​​​​A. Background & Definitions ==
 
+
to be added
tba
 
 
 
  
  
 
== B. Guidance & Expectations​ ==
 
== B. Guidance & Expectations​ ==
 
 
 
* must be knowledgeable to apply the needed principles of Good Research Practice to the study; responsible for execution of the study plan and appropriate documentation;
 
* must be knowledgeable to apply the needed principles of Good Research Practice to the study; responsible for execution of the study plan and appropriate documentation;
 
 
* effective communication to study director and quality professionals prior and during the study; especially study protocol deviations; communication of relevant health or medical conditions that may affect the study to appropriate person
 
* effective communication to study director and quality professionals prior and during the study; especially study protocol deviations; communication of relevant health or medical conditions that may affect the study to appropriate person
 
 
* responsibility for prompt recording of raw data after their generation in compliance with Good Research Practice and study protocol. Documentation of study plan deviations; seek training, as needed, to perform assigned study responsibilities. ​
 
* responsibility for prompt recording of raw data after their generation in compliance with Good Research Practice and study protocol. Documentation of study plan deviations; seek training, as needed, to perform assigned study responsibilities. ​
 
 
  
  
 
== ​C. Resources ==
 
== ​C. Resources ==
 
+
to be added
 
 
tba
 
 
 
  
  

Revision as of 12:35, 5 September 2020

​​​​A. Background & Definitions

to be added


B. Guidance & Expectations​

  • must be knowledgeable to apply the needed principles of Good Research Practice to the study; responsible for execution of the study plan and appropriate documentation;
  • effective communication to study director and quality professionals prior and during the study; especially study protocol deviations; communication of relevant health or medical conditions that may affect the study to appropriate person
  • responsibility for prompt recording of raw data after their generation in compliance with Good Research Practice and study protocol. Documentation of study plan deviations; seek training, as needed, to perform assigned study responsibilities. ​


​C. Resources

to be added



back to Toolbox

​Next item: 1.5.2.6 Supporting team