Clinical Research Nurse Job at Cedars-Sinai, Los Angeles, CA

V2FSdW91SktZRXdReVJaQzRlRlZlYVdk
  • Cedars-Sinai
  • Los Angeles, CA

Job Description

As a Research Nurse Coordinator , you’ll play a key role in the coordination and execution of clinical research studies. You will be the vital link between research participants, principal investigators, study sponsors, and our interdisciplinary care teams. This role offers a unique opportunity to combine your clinical expertise with research coordination, supporting innovative studies that may impact patient outcomes and the future of medicine.

Key Responsibilities:

  • Coordinate clinical study activities to ensure protocol adherence, regulatory compliance, and participant safety.
  • Act as a liaison between study participants, investigators, and research staff.
  • Educate patients and families on study protocols, clinical conditions, and disease processes.
  • Schedule and manage research participant visits and follow-ups.
  • Monitor and document adverse events and ensure proper reporting.
  • Collaborate with clinical teams to safely and effectively collect and document research data.
  • Present study information to interdisciplinary teams and ensure alignment with research goals.
  • Triage participant concerns by phone, providing appropriate clinical support.

Qualifications:

  • Associate Degree or Nursing Diploma required (BSN preferred).
  • Active RN license in the State of California.

Experience:

  • Research Nurse Coordinator I : 1–2 years of clinical nursing experience, with at least 1 year in a research setting (e.g., coordinating trials, working with protocols, engaging with IRBs, etc.).

  • Research Nurse Coordinator II : 2–3 years of clinical nursing experience, with at least 2 years in research setting , ideally within an academic medical center or industry-sponsored trial environment.

Experience may include:

  • Informed consent processes
  • Protocol development and study start-up
  • Clinical trial data entry and quality assurance
  • Regulatory submissions and sponsor interactions
  • Monitoring and documentation of patient safety and compliance

Job Tags

Similar Jobs

G-III Apparel Group

Production Associate | G-III Sports Job at G-III Apparel Group

 ...Production Associate | G-III Sports G-III Apparel Group New York, United States (On-site) Success Profile: The Production Associate...  ...product (garment) lifecycle from initial prototype to finished goods delivery. Drives daily development process through communication... 

MLM Hearing, LLC

Patient Care Coordinator Job at MLM Hearing, LLC

 ...flow and services to the patient. They support the clinical and home office staff by serving as the lead resource for office management...  ...retention calls as needed. The PCC will be required to travel to clinics that may be about 2 hours away 2 days a month, travel... 

Kelly Science, Engineering, Technology & Telecom

Clinical Study Assistant Job at Kelly Science, Engineering, Technology & Telecom

 ...Clinical Study Assistant Hybrid - On-site in Irvine, CA every Monday, Wednesday and every other Friday JOB GOAL: Provides administrative and organizational support for assigned clinical trials and sites in accordance with Good Clinical Practice (GCP), guidelines... 

Ladgov Corporation

Catholic Music Director & Musician Job at Ladgov Corporation

 ...Position: Catholic Music Director & Musician Location: Foothills Chapel, Beale AFB, CA Schedule: Sundays (2 hrs weekly), monthly Thursday rehearsal (2 hrs), ~9 special events/year Key Responsibilities: Provide music for weekly Catholic Mass, monthly choir... 

Source One Technical Solutions

Entry-level Drivers Job at Source One Technical Solutions

 ...Collection (Driver) Location: Los Angeles, CA Pay Rate: $25/hr (W-2) Shifts are available 7 days a week for weekdays or weekends Day Shift: 6:45am-3:15pm or 7:45am-4:15pm Night Shift: 2:45pm-11:15pm or 3:45pm-12:15am Wednesday-Sunday, Thursday-Monday...