Research Nurse I - Emergency Medicine (Full-Time, On-Site)
at CedarsSinai
Los Angeles, California, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 04 Dec, 2024 | USD 54 Hourly | 07 Sep, 2024 | N/A | Life Support | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
EDUCATIONAL REQUIREMENTS:
- Associate’s Degree / College Diploma in Nursing required
- Bachelor’s Degree in Nursing preferred
EXPERIENCE REQUIREMENTS:
- One (1) year of clinical nursing experience required
- One (1) year of research experience preferred
LICENSE & CERTIFICATION REQUIREMENTS:
- California State RN License required upon hire
- Basic Cardiac Life Support (BCLS) required upon hire
Jobs-Indeed
LI-On-site
ABOUT US
Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow’s health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents.
Responsibilities:
- Provides direct patient nursing care to research participants. Interacts with research participants to provide nursing care, administration of research interventions and specimen collection.
- Provides clinical education services to research participants and family regarding study participation, participants current clinical condition, and or disease process.
- Monitors research participant and reports potential adverse events to a member of the research team.
- Records research data (vital signs, research compound administered, participant responses) in approved source document (medical record, data collection sheet).
- Triages patient by phone and provides clinical information to the patient. May also coordinate patient visit to follow up on clinical issues and provide necessary care.
- Assists with recruitment and logistics of study participants.
- Completes and documents study participant enrollment, assessment/reassessment, education, and follow-up activities.
- Performs and coordinates study participant interventions as required.
- Serves as a liaison between study participants and PI or other research staff.
- Prepares data spreadsheets for Investigator and/or department.
- Completes Case Report Forms.
- Assists with data compilation and documentation
- May process, ship, track or otherwise handle research specimens.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Diploma
Proficient
1
Los Angeles, CA, USA