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UNIVERSITY OF SOUTHERN CALIFORNIA Lead Institutional Review Board Analyst Job Code: 121106OT Eligible:NoComp Approval:12/3/2020JOB SUMMARY: Leads the universitys Institutional Review Board (IRB) submission
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How to fill out lead institutional review board

01
To fill out a lead institutional review board, follow these steps:
02
Review the IRB application form provided by the institution.
03
Fill out the basic information section, including the project title, principal investigator's name, contact information, and project start and end dates.
04
Provide a detailed description of the research project, including its purpose, methodology, and any potential risks to participants.
05
Specify the target population or sample group for the research.
06
Outline the recruitment process and how potential participants will be informed and consented.
07
Include any measures taken to ensure the privacy and confidentiality of participants' personal information.
08
Describe the data collection procedures and methods used for analysis.
09
Address any potential conflicts of interest that may arise during the research.
10
Provide a clear plan for obtaining informed consent from participants.
11
Include any relevant supporting documents, such as research protocols, consent forms, or questionnaires.
12
Submit the completed lead institutional review board application to the designated department or office responsible for review.
13
Wait for the review board to assess and approve the application before proceeding with the research.

Who needs lead institutional review board?

01
Lead institutional review boards are typically needed by researchers or research organizations conducting studies involving human subjects.
02
This includes academic researchers, medical professionals, scientists, and graduate students.
03
Institutional review boards ensure that research involving human participants follows ethical guidelines and safeguards the well-being and rights of the participants.
04
These boards are often required by universities, hospitals, pharmaceutical companies, and other institutions conducting research.
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The Lead Institutional Review Board (IRB) is an independent committee established to review research proposals involving human subjects to ensure ethical standards and compliance with regulations.
Researchers and institutions conducting studies involving human subjects are required to file with the Lead IRB for review and approval before beginning their research.
To fill out the Lead IRB application, researchers must provide detailed information about the study, including objectives, methodology, participant recruitment, informed consent process, and potential risks.
The purpose of the Lead IRB is to protect the rights and welfare of human subjects involved in research by conducting thorough ethical reviews and ensuring compliance with regulatory standards.
Information that must be reported includes study title, principal investigator credentials, study protocol, consent forms, risk assessments, and any conflict of interest disclosures.
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