As an IRB Analyst I, you will work under the direct supervision of the Associate Director, IRB Operations and Education.
You will be primarily responsible for the management of a caseload of applications submitted for IRB review. In this capacity, you must demonstrate sound judgment, as well as analytical, organizational, and time management skills. The assigned job responsibilities require a firm foundation in the guidance and regulations that govern the inclusion of human subjects in research.
Your role will be to perform detailed analysis of all applications submitted for IRB review. Review each submission, verifying that all institutional requirements have been met, and determining whether applicable regulations and policies are appropriately addressed. You must consider the nature of the proposed research, make a determination regarding the necessary review process, and share this recommendation with the IRB reviewers. You will regularly attend IRB meetings to provide technical support and guidance on regulatory matters.
You will be expected to document the Board's determinations in the drafting of comprehensive meeting minutes and correspondence to investigators that effectively outline the concerns, rationale, and technical questions of the IRB. You are also responsible for conducting evaluations of investigator's response to identify potential issues for IRB reviewers and advise as to whether the requirements for IRB approval have been met. Likewise, you are responsible for documenting the review process thorough complete and timely entries in the IRB online submission and protocol tracking system.
You will serve as the primary point of contact with the research community. Utilizing your expertise in regulatory matters and IRB policies, assists investigators in the preparation of their IRB applications and informed consent forms.
You will participate in departmental quality improvement activities by identifying needs in department operations and making recommendations for their improvement as well as conduct special projects as assigned by the Director of the Research Compliance.
Providing healthcare for more than 100 years, Cedars-Sinai has evolved into one of the most dynamic and highly renowned medical centers in the world. Along with caring for patients, Cedars-Sinai is a hub for biomedical research and a training center for future physicians and other healthcare professionals. This attracts exceptional talent to Cedars-Sinai, including world-renowned physician-scientists who seek a place where they can both conduct research and see patients--the ideal formula for discovery and its translation into cures. Our patients benefit from access to doctors at the top of their fields, and our researchers have an ideal community in which to study the impact of healthcare challenges, and reflect that knowledge in their research. The greater Los Angeles area in which Cedars-Sinai resides possesses unparalleled cultural and ethnic diversity which offers outstanding opportunities for translational and clinical research... and a dynamic environment for medical education.Although community based, Cedars-Sinai is a major teaching hospital affiliated with the David Geffen School of Medicine at the University of California, Los Angeles (UCLA). Cedars-Sinai has highly competitive graduate medical education programs in more than 50 specialty and subspecialty areas, a graduate program in biomedical sciences and translational medicine, a clinical scholars program directed towards junior physicians with aspirations to become clinical scientists, and post graduate training opportunities.There are more than 250 full-time faculty members at Cedars-Sinai. The voluntary medical staff, comprised of more than 2,200 specialty board-certified or board-qualified physicians, represent all of the specialties and subspecialties and collaborate with full-time medical staff in the teaching responsibilities of the graduate medical education programs.