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Full-time

Clinical Research Coordinator I (Hybrid)

Competitive

Los Angeles, CAScience & PharmaceuticalPosted 20d ago

You'll complete your application on the employer's website.

Role overview

Job type

Full-time

Salary

Competitive

Posted

20 days ago

Job description

Responsibilities

Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process

Schedules patients for research visits and procedures

In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug

Maintains accurate source documents related to all research procedures

Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries

Schedules and participates in monitoring and auditing activities

Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings

Notifies direct supervisor about concerns regarding data quality and study conduct

Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines

May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation

Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board

Maintains research practices using Good Clinical Practice (GCP) guidelines

Maintains strict patient confidentiality according to HIPAA regulations and applicable law

Participates in required training and education programs

Preferred

Experience supporting behavioral research is preferred

Bachelor's Degree Science, Sociology or related degree - preferred

Certification In Clinical Research - Upon Hire preferred SOCRA or ACRP certification

Benefits

Hybrid work schedule, with a minimum requirement of 3 days onsite per week at the Los Angeles work location.

Opportunities to grow into new areas as projects evolve.

Opportunities to contribute to or lead manuscripts, abstracts, and conference presentations.

Glassdoor

3.9

Since its beginning in 1902, Cedars-Sinai has evolved to meet the healthcare needs of one of the most diverse regions in the nation, continually setting new standards for quality and innovation in patient care, research, teaching and community service.

Los Angeles, California, USA

https://www.cedars-sinai.org

Late Stage

Total Funding

$64.36M

Key Investors

Google.org

California Institute for Regenerative Medicine

American Academy of Orthopaedic Surgeons

2026-01-26

Grant

2025-05-29

Grant· $1.05M

2023-12-01

Grant· $0.01M

Leadership Team

Thomas Priselac

President/CEO

David Wrigley

Executive Vice President Finance, CFO and Treasurer

Recent News

PYMNTS.com

Hospitals Follow Banks’ Playbook for Taming Generic AI

2026-07-31

Qualifications

This role follows a hybrid work schedule, with a minimum requirement of 3 days onsite per week at our Los Angeles work location

Applicants must be able to meet this onsite requirement and, if hired, must reside within a commutable distance of the work location

The ideal candidate will have experience with data cleaning and REDCap database design and monitoring

High School Diploma/GED - minimum

1 year Clinical research related experience - minimum

No license or certification required - minimum

Experience supporting behavioral research is preferred

Bachelor's Degree Science, Sociology or related degree - preferred

Certification In Clinical Research - Upon Hire preferred SOCRA or ACRP certification

Required skills

Data Cleaning, REDCap Database Design and Monitoring, Clinical Research, Behavioral Research

Preferred skills

Experience supporting behavioral research is preferred

Experience

1+ years

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