Cancer-related research involving human subjects at the Cancer Institute of New Jersey (CINJ) submitted to the IRB require CINJ Scientific Review Board (SRB) approval before being eligible to receive IRB Approval.
CINJ Cancer-Related Human Subject Research
The Scientific Review Board (SRB) of the Cancer Institute of New Jersey (CINJ) is the institutional body charged with Protocol Review and Monitoring. The SRB oversees the scientific aspects of cancer-related research involving human subjects at the Cancer Institute of New Jersey (CINJ). The SRB focuses on the scientific merit of cancer-related research involving human subjects at CINJ. The function of the SRB is complementary to that of the Rutgers/RWJMS Institutional Review Board (IRB), but it does not duplicate or overlap the responsibilities of the IRB, which focuses on the protection of human subjects.
- Review the scientific merit of cancer-related research involving human subjects at CINJ.
- Review of amendments that are deemed to be significant to the scientific conduct and/or progress of the trial before IRB submission.
- Foster the development of innovative, collaborative, and scientifically sound studies, which focus on the prevention, detection, diagnosis, or treatment of cancer.
- Provide a standard format for submission and review.
- Review of trials identified by Human Research Oversight Committee (HROC) as having low accrual, significant toxicities or significant protocol violations.
- Close a trial when an accrual rate is judged too low to allow the aims of the trial to be completed within a reasonable period of time or if the scientific integrity of the trial is compromised due to the lack of adherence to the research design and methods of the protocol.
CINJ SRB Form Instructions
Please complete the following steps to submit your SRB application in the Oncore website.
- Access the Online Collaborative Research Environment (ONCORE) website. If you don’t have access to Oncore, please contact Yifang Zhou (CINJ).
- Once logged in, place your cursor over the tab ePRMS and click ‘Submission Console’.
- Look for the "Create Submission" section, on the left side of your screen, click the button for ‘Initial Review’. Begin entering information pertaining to your study. Please leave the protocol no. field blank, this will be entered by our in-house staff.
- After all requested and applicable information is entered, click ‘save’. An expanded version of the page will appear; the system will prompt you to provide additional information such as study team, study sites, sponsor and research documents.
- Review your information and make sure that you have entered as much information as possible, once done, click ‘submit’. This will send your application to the SRB coordinator to begin the review process.
CINJ SRB Help
- Director: Tracie Saunders 732-235-8861
- SRB Regulatory Manager: Merle Henry 732-235-9473
- SRB Coordinator: Doris Fonseca 732-235-7333