Job Description

Clinical Research Coordinator I - Heart Institute, Cheng Lab at CEDARS-SINAI summary:

The Clinical Research Coordinator I at Cedars-Sinai's Heart Institute manages various aspects of clinical research, including screening research participants, ensuring protocol compliance, and maintaining accurate documentation. This role involves collaborating with medical personnel and presenting findings at research meetings, while supporting significant studies aimed at improving kidney transplant outcomes. Ideal candidates possess clinical research experience, a high school diploma (or a bachelor's degree), and preferably certification from ACRP or SoCRA.

Job Description

Grow your career at Cedars-Sinai!

Cedars-Sinai offers a culture of happiness, passion, and dedication. This is one of the many reasons why we rank as one of the top hospitals in California and in the nation by U.S. News & World Report.

Do you have a passion for helping human kind?

The Clinical Research Coordinator I works independently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The incumbent will be responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. This position presents this information at research staff meetings and ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).

This position supports Kidney Transplant clinical research, which focuses on improving outcomes in transplant through development of interventions focused on quality of life, reducing surgery burden, improving early detection, and enhancing imaging techniques.

Primary Duties and Responsibilities:

• Schedules research visits and procedures for enrolled participants.
• In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in research participant condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
• Maintains accurate source documents related to all research procedures.
• Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information.
• Notifies direct supervisor about concerns regarding data quality and study conduct.

Department-Specific Responsibilities:

• Collects and documents specimens for translational studies.
• Performs study assessments.
• Collects wearable device data.
• Assess lean body mass.

Acquires quality of life data

Qualifications

Education:

• High School Diploma/GED is required.
• Bachelor's degree is preferred.

Licenses/Certifications:

• ACRP/SoCRA (or equivalent) certification is preferred.

Experience:

• One year of clinical research or coordinating clinical research trials experience is required.

Req ID : 5846
Working Title : Clinical Research Coordinator I - Heart Institute, Cheng Lab
Department : Heart Institute
Business Entity : Cedars-Sinai Medical Center
Job Category : Academic / Research
Job Specialty : Research Studies/ Clin Trial
Overtime Status : NONEXEMPT
Primary Shift : Day
Shift Duration : 8 hour
Base Pay : $23.39 - $39.76

Keywords:

Clinical Research Coordinator, Research Studies, Kidney Transplant, Clinical Trials, Data Collection, Protocol Compliance, Cedars-Sinai, Health Research, Informed Consent, Quality of Life Assessment

Job Tags

Local area, Shift work,

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