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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 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:

+ 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.

**Req ID** : 14260

**Working Title** : Research Nurse Coordinator I (Hybrid)

**Department** : Cancer - SOCCI Clinical Research

**Business Entity** : Cedars-Sinai Medical Center

**Job Category** : Nursing

**Job Specialty** : Research

**Overtime Status** : NONEXEMPT

**Primary Shift** : Day

**Shift Duration** : 8 hour

**Base Pay** : $40.03 - $60.05

Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.