Pediatric Clinical Research Coordinator II — Impactful Trials

Cedars-Sinai Medical Center - Los Angeles; Los Angeles (CA); On-site; USD 70,000 - 95,000; Full time

Job summary

Cedars-Sinai Medical Center - Los Angeles is seeking a Clinical Research Coordinator II to independently coordinate pediatric studies, screen patients for eligibility, present non-medical trial concepts, and participate in informed consent. You will ensure accurate source documents, data collection, entry, and sponsor communications.

Responsibilities include documenting on Case Report Forms, scheduling visits, coordinating with physicians and IRB, and maintaining HIPAA-compliant practices while

Qualifications

• High School Diploma/GED required.
• Two (2) years clinical research related experience required.
• SOCRA or ACRP certification preferred.

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.
• 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.
• Notifies direct supervisor about concerns regarding data quality and study conduct.
• Works with IRB to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters.

Skills

Clinical research

IRB coordination

Data collection

Education

Bachelor's degree in Science or related

SOCRA or ACRP certification

Tools

CRF documentation

Job description

Cedars-Sinai Medical Center - Los Angeles is seeking a Clinical Research Coordinator II to independently coordinate pediatric studies, screen patients for eligibility, present non-medical trial concepts, and participate in informed consent. You will ensure accurate source documents, data collection, entry, and sponsor communications.

Responsibilities include documenting on Case Report Forms, scheduling visits, coordinating with physicians and IRB, and maintaining HIPAA-compliant practices while