Cedars-Sinai
Research Nurse Coordinator III (10HR/Full-Time) - The Angeles Clinic & Research
Cedars-Sinai, Los Angeles, California, United States, 90079
Research Nurse Coordinator III, Full Time (Onsite) Angeles Clinic
Join to apply for the
Research Nurse Coordinator III, Full Time (Onsite) Angeles Clinic
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Cedars-Sinai Research Nurse Coordinator III, Full Time (Onsite) Angeles Clinic
1 week ago Be among the first 25 applicants Join to apply for the
Research Nurse Coordinator III, Full Time (Onsite) Angeles Clinic
role at
Cedars-Sinai Get AI-powered advice on this job and more exclusive features. Job Description
We’re excited to share an opportunity for a Job Description
We’re excited to share an opportunity for a
Research Nurse Coordinator III (Full-Time)
position! This is an
on-site role
with a
4/10 schedule , offering a great work-life balance. If you hold an
active RN license in California
and have
prior experience as a nurse working on clinical trials , we’d love for you to apply. We highly value
clinical research nurse experience , as you’ll play a key role in
supporting and coordinating clinical trials . A
SOCRA or ACRP certification
is required for the level III role—but if you don’t have one just yet, don’t worry! You may still be considered for a
level II position .
The Research Nurse Coordinator III is responsible for all activities associated with clinical study coordination, subject enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfacing with participants and family members. Coordinates the clinical logistics of the study, and works in tandem with the Research and/or Clinical Nurse who work to provide hands-on clinical care to the research participants. Utilizes clinical nursing background and extensive/complex research protocol knowledge to serve as liaison between nursing staff, Principal Investigator, other research staff, and study participants. Serves as a resource and mentor to the research staff by providing guidance, instruction, training, work-review and leading staff.
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 as reported by research participants, works closely with PI to document 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). Creates and presents education materials to the interdisciplinary team to on study requirements. Collaborates with the interdisciplinary team to create and communicate a plan of care. Triages patient by phone and provides clinical information to the patient. Completes and documents study participant enrollment, assessment/reassessment, education, and follow-up activities and ensures protocol is followed. Coordinates study participant tests and procedures as required. Prepares data spreadsheets for Investigator and/or department. Performs general oversight of research portfolio as it pertains to the clinical coordination of the studies. Serves as a resource and mentor to other research staff by providing training, work review and leading staff. Provides guidance, instruction and expertise to team members on study requirements and clinical coordination of the studies. May assist with grant proposals, publication preparation, and/or presentations. May process, ship, track or otherwise handle research specimens.
Qualifications
The Angeles Clinic and Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. We are committed to bringing innovative therapeutic options to all of our patients with cancer. As part of this commitment, our cancer clinical trials program has been expanded to include Experimental Therapeutics (Phase I) and Drug Development programs. With this commitment strengthened, we can continue to make advances in cancer care.
Requirements:
Bachelor's Degree Nursing or Health Science required. 5 years of Clinical Nursing & Research Experience required. Certification in Clinical Research SOCRA or ACRP required for a level III Research Nurse.
Preferred:
Master's Degree Nursing or Health Science preferred. Oncology experience preferred.
Req ID
: 10945
Working Title
: Research Nurse Coordinator III, Full Time (Onsite) Angeles Clinic
Department
: CMCF 1102083 Angeles Research Inst
Business Entity
: Cedars-Sinai Medical Care Foundation
Job Category
: Nursing
Job Specialty
: Research
Overtime Status
: NONEXEMPT
Primary Shift
: Day
Shift Duration
: 10 hour
Base Pay
: $49.66 - $79.46 Seniority level
Seniority level Not Applicable Employment type
Employment type Full-time Job function
Job function Health Care Provider Industries Hospitals and Health Care, IT Services and IT Consulting, and Research Services Referrals increase your chances of interviewing at Cedars-Sinai by 2x Sign in to set job alerts for “Clinical Research Nurse” roles.
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We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Join to apply for the
Research Nurse Coordinator III, Full Time (Onsite) Angeles Clinic
role at
Cedars-Sinai Research Nurse Coordinator III, Full Time (Onsite) Angeles Clinic
1 week ago Be among the first 25 applicants Join to apply for the
Research Nurse Coordinator III, Full Time (Onsite) Angeles Clinic
role at
Cedars-Sinai Get AI-powered advice on this job and more exclusive features. Job Description
We’re excited to share an opportunity for a Job Description
We’re excited to share an opportunity for a
Research Nurse Coordinator III (Full-Time)
position! This is an
on-site role
with a
4/10 schedule , offering a great work-life balance. If you hold an
active RN license in California
and have
prior experience as a nurse working on clinical trials , we’d love for you to apply. We highly value
clinical research nurse experience , as you’ll play a key role in
supporting and coordinating clinical trials . A
SOCRA or ACRP certification
is required for the level III role—but if you don’t have one just yet, don’t worry! You may still be considered for a
level II position .
The Research Nurse Coordinator III is responsible for all activities associated with clinical study coordination, subject enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfacing with participants and family members. Coordinates the clinical logistics of the study, and works in tandem with the Research and/or Clinical Nurse who work to provide hands-on clinical care to the research participants. Utilizes clinical nursing background and extensive/complex research protocol knowledge to serve as liaison between nursing staff, Principal Investigator, other research staff, and study participants. Serves as a resource and mentor to the research staff by providing guidance, instruction, training, work-review and leading staff.
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 as reported by research participants, works closely with PI to document 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). Creates and presents education materials to the interdisciplinary team to on study requirements. Collaborates with the interdisciplinary team to create and communicate a plan of care. Triages patient by phone and provides clinical information to the patient. Completes and documents study participant enrollment, assessment/reassessment, education, and follow-up activities and ensures protocol is followed. Coordinates study participant tests and procedures as required. Prepares data spreadsheets for Investigator and/or department. Performs general oversight of research portfolio as it pertains to the clinical coordination of the studies. Serves as a resource and mentor to other research staff by providing training, work review and leading staff. Provides guidance, instruction and expertise to team members on study requirements and clinical coordination of the studies. May assist with grant proposals, publication preparation, and/or presentations. May process, ship, track or otherwise handle research specimens.
Qualifications
The Angeles Clinic and Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. We are committed to bringing innovative therapeutic options to all of our patients with cancer. As part of this commitment, our cancer clinical trials program has been expanded to include Experimental Therapeutics (Phase I) and Drug Development programs. With this commitment strengthened, we can continue to make advances in cancer care.
Requirements:
Bachelor's Degree Nursing or Health Science required. 5 years of Clinical Nursing & Research Experience required. Certification in Clinical Research SOCRA or ACRP required for a level III Research Nurse.
Preferred:
Master's Degree Nursing or Health Science preferred. Oncology experience preferred.
Req ID
: 10945
Working Title
: Research Nurse Coordinator III, Full Time (Onsite) Angeles Clinic
Department
: CMCF 1102083 Angeles Research Inst
Business Entity
: Cedars-Sinai Medical Care Foundation
Job Category
: Nursing
Job Specialty
: Research
Overtime Status
: NONEXEMPT
Primary Shift
: Day
Shift Duration
: 10 hour
Base Pay
: $49.66 - $79.46 Seniority level
Seniority level Not Applicable Employment type
Employment type Full-time Job function
Job function Health Care Provider Industries Hospitals and Health Care, IT Services and IT Consulting, and Research Services Referrals increase your chances of interviewing at Cedars-Sinai by 2x Sign in to set job alerts for “Clinical Research Nurse” roles.
Registered Nurse - Pediatric Ambulatory Care
Long Beach, CA $77,580.00-$161,878.00 1 week ago Los Angeles, CA $78,000.00-$151,000.00 2 weeks ago Glendale, CA $2,607.00-$2,607.00 2 days ago Glendale, CA $2,607.00-$2,607.00 1 day ago Inglewood, CA $83,200.00-$83,200.00 7 months ago RN Clinical - 5 S ICU - Part Time 12 Hour Days (Non-Exempt) (Union)
Los Angeles, CA $71,000.00-$151,000.00 1 month ago Ambulatory Care Center Registered Nurse (RN)
Registered Nurse - Clinical Research (Night Shift)
Supervisor of Nursing Clinical Research RN
RN Clinical - 5 S ICU - Part Time 12 Hour Days (Non-Exempt) (Union)
Supervisor of Nursing Clinical Research RN
Clinic RN, Oncology - Todd Cancer Institute Specialty
San Pedro, CA $60,000.00-$118,000.00 2 weeks ago RN, Clinical Practice & Education - Clinical Educator NICU
Registered Nurse - Clinical Documentation Specialist - 8 Hour Days
Registered Nurse - Infection Preventionist
Registered Nurse - Case Management Coordinator
Registered Nurse - Outpatient Oncology Clinic
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr