Surgery Clinical Research Coordinator II — Drive Trials

Cedars-Sinai; Los Angeles (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

Cedars-Sinai in Los Angeles seeks a Clinical Research Coordinator II to independently coordinate studies, screen patients for eligibility, and contribute to consent processes. You will maintain accurate data and source documents, respond to sponsor queries, and assist with IRB and regulatory duties as needed.

Responsibilities include scheduling visits, documenting case report forms, reporting on protocol activity, and helping identify opportunities to improve enrollment and efficiency while

Qualifications

• 2 years clinical research experience required.
• SOCRA or ACRP certification preferred.
• Bachelor's degree in science, sociology or related field preferred.
• High School Diploma/GED required.

Responsibilities

• Coordinate screening of potential patients for protocol eligibility.
• Document and report data from study visits and adverse events.
• Assist with informed consent process and regulatory submissions.
• Maintain source documents and ensure data accuracy for sponsor queries.
• Collaborate with investigators and coordinators to improve enrollment and study efficiency.
• Comply with FDA and IRB requirements and Good Clinical Practice (GCP).

Education

High School Diploma/GED

Bachelor's Degree in Science, Sociology or related degree

Job description

Cedars-Sinai in Los Angeles seeks a Clinical Research Coordinator II to independently coordinate studies, screen patients for eligibility, and contribute to consent processes. You will maintain accurate data and source documents, respond to sponsor queries, and assist with IRB and regulatory duties as needed.

Responsibilities include scheduling visits, documenting case report forms, reporting on protocol activity, and helping identify opportunities to improve enrollment and efficiency while