Clinical Research Coordinator I — Study Coordination Pro

Cedars-Sinai; Los Angeles (CA); On-site; USD 65,000 - 85,000; Full time

Job summary

Cedars-Sinai in Los Angeles seeks a Clinical Research Coordinator I to coordinate studies, screen patients for protocol eligibility, and participate in the informed consent process. You will ensure accurate source documents, data collection, and timely reporting to sponsors.

You will work with physicians and staff to document on CRFs, manage adverse events, and support monitoring and regulatory activities while maintaining HIPAA and GCP standards.

Qualifications

• High School Diploma or GED required; Bachelor's degree in Science, Sociology or related field preferred.
• 1 year of clinical research experience required; 2–3 years preferred.
• SOCRA or ACRP certification preferred upon hire.

Responsibilities

• Coordinate studies independently, screen patients for protocol eligibility, and participate in informed consent.
• Schedule patients for research visits and procedures.
• Document on Case Report Forms changes in patient condition, adverse events, and protocol compliance.
• Maintain accurate source documents for all research procedures.
• Ensure accurate data collection, documentation, entry, and sponsor query responses.
• Schedule and participate in monitoring and auditing activities.
• Compile and report study information at staff meetings and share updates with supervisors.
• Notify supervisor about data quality or study conduct concerns.
• Work with IRB/regulatory team to submit adverse events and safety letters as required.

Skills

Study coordination

Data collection

Regulatory compliance

GCP

HIPAA

Education

High School Diploma/GED

Bachelor's degree in Science, Sociology or related

SOCRA or ACRP certification

Job description

Cedars-Sinai in Los Angeles seeks a Clinical Research Coordinator I to coordinate studies, screen patients for protocol eligibility, and participate in the informed consent process. You will ensure accurate source documents, data collection, and timely reporting to sponsors.

You will work with physicians and staff to document on CRFs, manage adverse events, and support monitoring and regulatory activities while maintaining HIPAA and GCP standards.