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IRB 101: An Investigator Handbook Research Administration Office TABLE OF CONTENTS Introduction....page 4 University of Arizona Policies....page 4 What Is The Basis for The Ethical and Regulatory
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How to fill out IRB 101 as an investigator?

01
Start by reading the instructions: Before filling out the IRB 101 form, carefully read the provided instructions. These instructions will provide you with important guidance on how to complete the form accurately.
02
Provide Personal Information: Begin by providing your personal information such as your full name, contact details, affiliation, and any relevant credentials.
03
Specify the Research Title: Clearly state the title of your research project. Make sure it accurately reflects the purpose and scope of your study.
04
Describe the Research Objectives: Briefly outline the main goals and objectives of your research. This will help the IRB members understand the significance and potential impact of your study.
05
Explain the Research Design: Provide a clear description of your research design, including the methodologies, data collection methods, and analysis techniques you intend to use. This section should provide enough detail to help the IRB members evaluate the ethical implications of your research.
06
Discuss Participant Recruitment: Detail how you plan to recruit participants for your study. Include information about the target population, the recruitment methods, and any incentives or compensation offered to participants.
07
Address Potential Risks and Benefits: Identify any potential risks that participants might face while taking part in your study. Additionally, highlight any potential benefits that may arise from your research.
08
Describe Informed Consent Procedures: Clearly explain how you plan to obtain informed consent from participants. Discuss the consent process, including any written consent forms, information provided to participants, and any additional steps taken to ensure participants understand the study and their rights.
09
Outline Confidentiality and Data Privacy Measures: Describe how you plan to handle and protect the confidentiality of participant data. Explain any measures taken to ensure data privacy and security throughout the research process.
10
Provide Relevant Supporting Documents: Attach any relevant supporting documents as per the IRB's requirements. These may include consent forms, recruitment materials, questionnaires, or any other documents that support your research application.

Who needs IRB 101 as an investigator?

Researchers who are planning to conduct studies involving human participants need to complete IRB 101 as part of the Institutional Review Board (IRB) process. This includes researchers from various disciplines such as social sciences, medicine, psychology, and education. The IRB's primary role is to review and approve the ethical conduct of research to ensure the protection of participants' rights, safety, and welfare. Completing IRB 101 is essential to demonstrate the researcher's understanding of ethical considerations and their commitment to conducting responsible and ethical research involving human subjects.
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IRB 101 for an investigator is a form used to provide information on the researcher responsible for a particular research study.
Investigators conducting research studies that involve human subjects are required to file IRB 101.
The IRB 101 form typically requires information on the investigator's background, qualifications, experience, and any potential conflicts of interest.
The purpose of IRB 101 for an investigator is to ensure that researchers conducting studies involving human subjects are qualified and have the necessary expertise to carry out the research ethically and responsibly.
Information such as the investigator's credentials, past research experience, and any conflicts of interest must be reported on IRB 101.
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