Clinical Trials Compliance

If you are looking for information on industry-sponsored or privately funded clinical trials, please contact the Research Compliance Mailbox.  

What is a Clinical Trial?

In 2015, NIH changed the definition of clinical trial to “A research study in which one or more human subjects are prospectively assigned to one or more interventions (which may include placebo or other control) to evaluate the effects of those interventions on health-related biomedical or behavioral outcomes.”

To qualify as a clinical trial, a study must meet all of these criteria. Research that involves individuals who are no longer living, studies of existing biological specimens collected for another purpose, or research that seeks to define an existing measure are some examples of studies that are not clinical trials.

If you aren’t sure whether or not your study is a clinical trial, use the NIH Decision Tool. 

NIH Single IRB (sIRB) Requirement

An NIH-funded clinical trial being conducted at more than one site within the U.S. may be subject to the NIH Single IRB policy. This policy does not apply to non-U.S. sites.  There are also certain NIH awards that are exempt from this policy, specifically career development (K), institutional training (T), and fellowship (F) awards.  

Any IRB that serves at the sIRB of record for NIH-sponsored research must be registered with the HHS Office of Human Research Protections (OHRP) and must have adequate expertise to review the proposed study.

Please note that the 菠菜网lol正规平台 IRB is not currently registered to serve as the sIRB of record for multi-site NIH-sponsored research. You may use an institutional IRB that is associated with a co-investigator, one of the participating sites, or a commercial IRB. It is very important that you work with your co-investigators to identify an sIRB as early in the proposal process as possible, as there may be costs associated with sIRB review. These costs should be included in your budget.

Training in Good Clinical Practice

You must have training in Good Clinical Practice (GCP) if you are an investigator or clinical trial staff responsible for the conduct, management, or oversight of an NIH-funded clinical trial. Clinical trial staff members include research coordinators, study coordinators, co-investigators or students.  

CGP training is meant to ensure that the rights, safety, and well-being of human subjects are protected and the trial is conducted with rigor and integrity. It is also intended to ensure that investigators are trained in how to collect reliable data.  

菠菜网lol正规平台 provides investigators with access to GCP training through the Collaborative Institutional Training Initiative (CITI). To access the GCP training:

  • Visit the CITI website
  • Log in, or create an account using your 菠菜网lol正规平台 email address
  • Select “San Jose State University Courses”
  • Click on “add a course or update learner groups”
  • Answer the required questions, and check the box in Question 4, “Good Clinical Practice (GCP)”

Proof of GCP training should be included in the study documentation and must be repeated at least every three years.  

ClinicalTrials.gov Registration and Reporting

All clinical trials funded in whole or in part by NIH must be registered at clinicaltrials.gov. You must also submit the results of the trial on the site.

菠菜网lol正规平台 has an institutional account for clinicaltrials.gov, but you will need an individual user account to register the study. Contact the Research Compliance Mailbox to obtain this user account.  

You will need your IRB approval number and a copy of your IRB-approved consent form to register your study - please ensure that your study has been approved by the 菠菜网lol正规平台 IRB prior to requesting your clinicaltrials.gov user account.

ResearchMatch for 菠菜网lol正规平台 Researchers

Access to ResearchMatch is granted on a study-by-study basis; that is, investigators must individually register each study. Registration takes only a few minutes and you must complete the process in one sitting.

There are two levels of access available to 菠菜网lol正规平台 investigators: feasibility access and recruitment access.

Investigators may sign themselves up in ResearchMatch or may delegate recruitment privileges to a study coordinator or other study team member (a proxy).

Feasibility access

Feasibility access gives you the ability to view aggregate data on the registry population without an IRB-approved protocol. To register a study for feasibility access, you must:

  • Be affiliated with 菠菜网lol正规平台
  • Provide your 菠菜网lol正规平台 email address
  • Create a ResearchMatch username and password

Recruitment access

Recruitment access gives you the ability to recruit volunteers through ResearchMatch. To register a study for recruitment access, you must meet the same access requirements as for feasibility access. In addition, for each study you want to recruit for, you must:

  • Be the principal investigator (PI) or authorized to recruit for the study on behalf of the PI
  • Upload an electronic copy of your IRB approval letter, and an IRB-approved recruitment message to implement when using ResearchMatch.

Note: Individuals accessing as a proxy for the PI will be asked to indicate that, and to provide the study PI’s name, email address and phone number.