Clinical Research Courses: Responsibilities of Principle Investigator

Posted by raveena aher on April 13th, 2021

Students do learn about the significance of clinical trials and research studies. In clinical research courses. However, we wonder if they are aware as to why many staff is needed in a single trial.  The main reasons for the requirement of various staff are the extra responsibilities that need to be fulfilled during a study or a trial. Students will learn about these responsibilities as well in their clinical research courses.

Who is the Principle Investigator as told by Clinical Research Courses?

Research studies often have a Lead Investigator who would have completed their clinical research courses after their bachelor’s degree. These individuals have primary responsibility in the entire trial. Moreover, The Lead Investigator is no other than the Principal Investigator (PI) at the lead research site.  In multicenter trials, there are several research sites which have their own Principal Investigator who oversee different responsibilities as well as staff included in the administration of these studies. One gets to know more about Principal Investigator in detail during clinical research courses.

What are the responsibilities of the Principal Investigator (PI?)

The Principal Investigator (PI) has various responsibilities during the conduct of research studies and clinical trials. Clinical research courses would tell one about the key responsibilities that the PI has throughout the trial. Even though there are various staff members for carrying out particular responsibilities. The PI would have the following responsibilities:

  •         Recording the delegation of study responsibilities to qualified and trained research staff.
  •         Overseeing study performance and managing the performance of study staff
  •         At the research sites.
  •         Making a communication plan for all staff involved in the study.
  •         Confirming Participants’ well-being and safety
  •          Guaranteeing that all study procedures at the research sites are conducted in accordance with the protocol and GCP.
  •         Supervision of  Investigational product accountability

Students will learn more about these responsibilities in their clinical research courses.

https://www.technobridge.in/clinical-research-course.html    

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raveena aher

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raveena aher
Joined: April 2nd, 2021
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