At Cedars-Sinai, we're motivated by a collective spirit of innovation and the challenge to continuously improve. Above all, we share a real passion for helping others. Day after day, from department to department, our people give their all to create a community unlike any other. This is just one of the many reasons U.S. News & World Report has named us one of America's Best Hospitals--and now we invite you to join us and make a difference every single day in service of this outstanding work - excellence and innovation in patient care, research, and community service. From working with a team of dedicated professionals to using state-of-the-art facilities, you'll have great resources to do something incredible--for yourself, and for others.

Join our team and expand your skills and knowledge!

The CRC II will conduct pre-screening, in-person recruitment, participant follow-up, visit coordination, participant binder preparation, specimen kit preparation, kit inventory, data entry, data verification, letters/mailings, phone calls, ordering supplies, and other duties as assigned. We're seeking a highly motivated individual interested in cancer epidemiological research. The ideal candidate is team-oriented with a hardworking and positive demeanor, must possess excellent communication and organizational skills, strong interpersonal skills, and willingness to excel in a fast-paced, team environment.

Essential job duties and responsibilities:

• Independent study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details to the research participants, and participating in the informed consent process.
• Scheduling of research participants for research visits and procedures.
• Documents thoroughly on Case Report Forms (CRFs) the following; changes in research participant condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
• Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries.
• Responsible 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.
• Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit initial applications, amendments, continuing reviews, Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
• May involve other regulatory / Institutional Review Board duties, budgeting duties, and assisting with research participant billing and reconciliation.
• Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board.)
• Maintains strict research participant confidentiality according to HIPAA regulations and applicable law.
• Plans and coordinates strategies for increasing research participant enrollment, and/or improving clinical research efficiency.
• Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality.
• Participates in required training and education programs.

• Working Title: Clinical Research Coordinator II - Research Center for Health Equity
• Department: Research Center Health Equity
• Business Entity: Academic / Research
• City: West Hollywood
• Job Category: Academic/Research
• Job Specialty: Research Studies/Clinical Trials
• Position Type: Full-time
• Shift Length: 8 hour shift
• Shift Type: Day