Cedars-Sinai
Research Nurse Coordinator III - $5,000 Sign-On Bonus!
Cedars-Sinai, Beverly Hills, California, United States, 90211
Research Nurse Coordinator III - $5,000 Sign-On Bonus!
Full‑time, on‑site role with a 4/10 schedule offering a great work‑life balance. This position requires an active RN license in California and prior experience working in clinical trials. A SOCRA or ACRP certification is required at the Level III level; candidates without certification may be considered for a Level II position.
Base Pay Range $50.66/hr – $81.06/hr
About the Role The Cedars‑Sinai Research and Clinical Trials Institute is committed to pioneering innovative cancer therapies. The Research Nurse Coordinator III supports and coordinates clinical trials, ensuring protocol adherence, regulatory compliance, and excellent participant care.
What You'll Be Doing • Coordinate all clinical study activities, including subject enrollment, data management, and study logistics. • Serve as a liaison between participants, the Principal Investigator, and research staff. • Provide education to participants and families about the study and disease process. • Document adverse events, maintain study records, and report to regulatory authorities and sponsors. • Create and present education materials for the interdisciplinary team. • Collaborate on the development and communication of care plans. • Triage patient inquiries by phone and provide clinical information. • Ensure all study procedures and tests are completed according to protocol. • Mentor and train research staff, providing guidance, work review, and leadership. • Assist with grant proposals, publication preparation, and specimen handling as needed.
Primary Duties and Responsibilities
Coordinate clinical study activities and maintain protocol adherence.
Provide educational services to participants and families.
Assess and document adverse events in collaboration with the PI.
Record study data and present education materials to the team.
Collaborate on care plans and triage patient inquiries by phone.
Document enrollment, assessments, education, and follow‑up activities.
Coordinate study participant tests and procedures.
Oversee the research portfolio in the clinical coordination of studies.
Mentor and train research staff on study requirements.
Assist with grant proposals, publication preparation, and presentations.
Process, ship, track, or otherwise handle research specimens.
Requirements
Bachelor's Degree in Nursing or Health Science.
At least 5 years of Clinical Nursing & Research Experience.
Valid California RN license.
Basic Life Support (BLS) certification from the American Heart Association or American Red Cross.
Certification in Clinical Research (SOCRA or ACRP) required for Level III position.
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Base Pay Range $50.66/hr – $81.06/hr
About the Role The Cedars‑Sinai Research and Clinical Trials Institute is committed to pioneering innovative cancer therapies. The Research Nurse Coordinator III supports and coordinates clinical trials, ensuring protocol adherence, regulatory compliance, and excellent participant care.
What You'll Be Doing • Coordinate all clinical study activities, including subject enrollment, data management, and study logistics. • Serve as a liaison between participants, the Principal Investigator, and research staff. • Provide education to participants and families about the study and disease process. • Document adverse events, maintain study records, and report to regulatory authorities and sponsors. • Create and present education materials for the interdisciplinary team. • Collaborate on the development and communication of care plans. • Triage patient inquiries by phone and provide clinical information. • Ensure all study procedures and tests are completed according to protocol. • Mentor and train research staff, providing guidance, work review, and leadership. • Assist with grant proposals, publication preparation, and specimen handling as needed.
Primary Duties and Responsibilities
Coordinate clinical study activities and maintain protocol adherence.
Provide educational services to participants and families.
Assess and document adverse events in collaboration with the PI.
Record study data and present education materials to the team.
Collaborate on care plans and triage patient inquiries by phone.
Document enrollment, assessments, education, and follow‑up activities.
Coordinate study participant tests and procedures.
Oversee the research portfolio in the clinical coordination of studies.
Mentor and train research staff on study requirements.
Assist with grant proposals, publication preparation, and presentations.
Process, ship, track, or otherwise handle research specimens.
Requirements
Bachelor's Degree in Nursing or Health Science.
At least 5 years of Clinical Nursing & Research Experience.
Valid California RN license.
Basic Life Support (BLS) certification from the American Heart Association or American Red Cross.
Certification in Clinical Research (SOCRA or ACRP) required for Level III position.
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