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Research Nurse Coordinator ; Hybrid

Job in Beverly Hills, Los Angeles County, California, 90211, USA
Listing for: Cedars-Sinai
Full Time position
Listed on 2026-01-05
Job specializations:
  • Nursing
    RN Nurse, Clinical Research Nurse
Job Description & How to Apply Below
Position: Research Nurse Coordinator I (Hybrid)

Job Description

The Research Nurse Coordinator I is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfaces with participants and family members. Coordinates the clinical logistics of the study, and works in tandem with the Research and/or Clinical Nurse who provide hands‑on clinical care to research participants. Utilizes clinical nursing background and basic research protocol knowledge to serve as a liaison between nursing staff, Principal Investigator, other research staff, and study participants.

Primary

Duties and Responsibilities
  • Responsible for clinical study activities, coordination, adherence to protocols and serves as a liaison between study participants, Principal Investigator (PI), and other research staff.
  • Provides educational services to research participants and family regarding study participation, participants current clinical condition, and or disease process.
  • Assesses and documents adverse events reported by research participants, informs PI, and documents according to department process (grade, attribution, treatment, etc), and reports to regulatory and sponsor as required.
  • Records research data where assessed or reported by patient (i.e. symptoms of treatment).
  • Presents education materials to the interdisciplinary team on study requirements.
  • Collaborates with the interdisciplinary team and communicates a plan of care that allows for safe and effective collection of clinical research data.
  • Schedules research participant study visits.
  • Triages patient by phone and provides clinical information to the patient.
  • Completes and documents study participant enrollment, assessment/reassessment, education, and follow‑up activities.
  • Coordinates study participant tests and/or procedures as required and ensures protocol is followed.
  • May prepare IRB submissions.
  • May process, ship, track or otherwise handle research specimens.
Qualifications

Required:
  • Associate. Degree/College Diploma Nursing required.
  • 2 years of Clinical Nursing Experience required.
  • RN State License California RN license Upon Hire.
  • Basic Life Support Upon Hire.
Preferred:
  • Bachelor's Degree Nursing or Health Science preferred.
  • 1 year Clinical research experience preferred.
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