Hybrid Clinical Research Coordinator II - Trials

CEDARS-SINAI; Los Angeles (CA); Hybrid; USD 70,000 - 90,000; Full time

Job summary

Cedars-Sinai is seeking a Clinical Research Coordinator II in Los Angeles. The position supports a hybrid schedule with four days onsite and one day remote, and may require additional onsite presence per patient needs and study priorities.

The role involves independent study coordination, screening patients for eligibility, obtaining consent, data collection, and reporting to sponsors. Experience with multiple EDC systems and GCP/IRB compliance is expected.

Qualifications

• Experience coordinating clinical trials across multiple EDC systems.
• Attention to data accuracy and timelines.
• Oncology trial experience preferred but not required.

Responsibilities

• Screen potential patients for protocol eligibility and discuss trial concepts.
• Schedule patients for research visits and procedures.
• Document changes in Case Report Forms (CRFs) including adverse events.
• Maintain accurate source documents for all procedures.
• Respond to sponsor queries with timely data reporting.
• Coordinate monitoring and auditing activities.
• Present study information at research staff meetings.
• Ensure compliance with GCP, FDA and IRB requirements.
• Coordinate training and education of personnel.

Skills

GCP (Good Clinical Practice)

HIPAA compliance

data management

IRB coordination

EDC systems

Education

High School Diploma/GED

Bachelor's Degree in Science/Sociology or related

Tools

EDC systems

Job description

Cedars-Sinai is seeking a Clinical Research Coordinator II in Los Angeles. The position supports a hybrid schedule with four days onsite and one day remote, and may require additional onsite presence per patient needs and study priorities.

The role involves independent study coordination, screening patients for eligibility, obtaining consent, data collection, and reporting to sponsors. Experience with multiple EDC systems and GCP/IRB compliance is expected.