Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements. Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of researchers develop some of the most advanced clinical trials in the world. Here, you will be a part of leading-edge cancer research history that improves and enhances our patients' treatment options, one trial at a time.
Do you have a passion for helping human kind?
As Clinical Research Coordinator (CRC) II, you will provide independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process. Your work will support our mission of rapidly translating research discoveries into safe, effective treatments.
You will work in collaboration with Clinical Research Associates, Research Program Administrators and Research Nurse Coordinators.
As a CRC II, you will also be responsible for the following:
Working with the physician and other medical personnel, you will document changes in patient conditions, adverse events, concomitant medication use, protocol compliance, response to study drug.
Works independently providing study coordination, including the screening of new research participants.
Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries.
Schedule patients for research visits and procedures and participate in monitoring and auditing activities
Accountable for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
Work closely with a regulatory coordinator or directly with (IRB) to submit adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in conjunction with local and federal guidelines.
Be involved with other regulatory duties such as: budgeting duties and assisting with patient research billing and reconciliation.
Plan and coordinate strategies for increasing patient enrollment.
You will ensure compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board.
You will maintain research practices using Good Clinical Practice (GCP) guidelines and maintain strict patient confidentiality according to HIPAA regulations and applicable law
This position is eligible for the Employee Referral Program. See website for details: http://careers.cedars-sinai.edu/working-here/employee-referrals/
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.