Get the free Investigator Site Questionnaire - UNC Research

Investigator Site Questionnaire Submit this form directly to CIRB via Connexus Important: Please type responses. Refer to the CIRB Investigator Guidebook for information regarding Investigator Responsibilities.

How to fill out investigator site questionnaire

How to fill out an investigator site questionnaire?

1. Read the questionnaire thoroughly: Start by carefully reading the investigator site questionnaire to understand the purpose and requirements. This will give you an overview of what information needs to be provided.
2. Gather necessary documents: Collect all the relevant documents and information needed to complete the questionnaire. This may include site-specific protocols, previous research experience, qualifications of staff, certifications, and any other supporting documentation.
3. Provide accurate and complete information: Fill out each section of the questionnaire accurately and provide complete information. Ensure that all information is up-to-date and relevant to your site.
4. Review your answers: Once you have completed filling out the questionnaire, take a moment to review your answers. Double-check for any errors or missing information. Also, ensure that your answers are consistent and align with the specific guidelines provided.
5. Submit the questionnaire: Finally, submit the filled-out investigator site questionnaire as instructed. Make sure to follow the specified submission method and meet any stated deadlines.

Who needs an investigator site questionnaire?

1. Clinical trial sponsors: The primary purpose of an investigator site questionnaire is to gather information about potential research sites. Clinical trial sponsors need this information to evaluate the suitability of a site for conducting a specific study. They use the questionnaire responses to assess the site's capabilities, resources, and expertise.
2. Investigators and research sites: Investigators and research sites themselves may be required to fill out an investigator site questionnaire. This allows them to provide detailed information about their facility, staff, capabilities, and previous experience with clinical trials. It helps them showcase their qualifications and suitability for participating in the study.
3. Regulatory authorities: Regulatory authorities also rely on investigator site questionnaires to evaluate the capabilities and compliance of research sites. These questionnaires help regulatory authorities determine if a site meets the necessary standards and requirements to conduct clinical research. It ensures the protection of patient rights, data integrity, and overall study quality.

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What is investigator site questionnaire?

It is a document that collects essential information about a clinical trial site, including facilities, staff qualifications, and capability to conduct the study.

Who is required to file investigator site questionnaire?

The principal investigator or lead research team at each clinical trial site is typically responsible for completing and filing the investigator site questionnaire.

How to fill out investigator site questionnaire?

The investigator site questionnaire can usually be completed online or in a specific format provided by the sponsor or regulatory authority. It requires detailed information about the site's capabilities, resources, and experience.

What is the purpose of investigator site questionnaire?

The purpose of the investigator site questionnaire is to assess the suitability of a clinical trial site and ensure it meets the necessary standards to conduct the study effectively and ethically.

What information must be reported on investigator site questionnaire?

The questionnaire typically requires information on the site's facilities, equipment, staff qualifications, previous experience in clinical research, and adherence to Good Clinical Practice (GCP) guidelines.