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Open nowPosted today

Clinical Research Nurse Coordinator I - Hybrid

Cedars-Sinai904 open roles

Where
Beverly Hills, CA, United States
Work mode
Hybrid
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Your applicationOpen nowClinical Research Nurse Coordinator I - HybridCedars-Sinai · Beverly Hills, CA, United States

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The clock on this job

Early applications get read.

13.9% of postings close within 7 days. Measured by our own scanner across the market. Cedars-Sinai postings stay open a median of 20 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.7%3 days
  3. 13.9%7 days
  4. 22.4%14 days
  5. 38.1%30 days
  6. 59.0%60 days
This job: posted today

Cedars-Sinai median: 20 days open

The posting

Job Description

Thank you for your interest in the Research Nurse Coordinator I opportunity! We want to be transparent about a few key requirements to help ensure the role is the right fit. While this position is designated as hybrid, it requires being onsite 4 days per week, so candidates must reside in the Los Angeles area and be able to consistently meet the onsite schedule.

Most importantly, this role requires a minimum of 2 years of clinical research nursing experience. Candidates must have nursing experience specifically within a clinical research environment, supporting research participants and the clinical components of research studies or trials. General bedside or patient-care nursing experience alone would not meet this requirement.

Candidates must also hold an active California Registered Nurse (RN) license upon hire.

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.

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 communicate 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 Qualifications

  • Associate Degree or College Diploma in Nursing.
  • Minimum of 2 years of clinical nursing experience specifically within a clinical research environment, supporting research participants and the clinical components of research studies or trials. General bedside or patient-care nursing experience alone does not meet this requirement.
  • Current California RN license upon hire.
  • Basic Life Support (BLS) certification upon hire.

Preferred Qualifications

  • Bachelor's Degree in Nursing or Health Science.
  • Minimum of 1 year of clinical research experience.
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