Clinical Research Coordinator I (Hybrid)
Competitive
You'll complete your application on the employer's website.
Competitive
You'll complete your application on the employer's website.
Job type
Salary
Competitive
Location
Sector
Posted
20 days ago
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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