Hybrid Clinical Research Coordinator II - Impact & Compliance

Cedars-Sinai; Beverly Hills (CA); Hybrid; USD 65.000 - 85.000; Vollzeit

Zusammenfassung

Cedars-Sinai in Los Angeles is hiring a Clinical Research Coordinator II for a hybrid role requiring four on-site days per week. The coordinator will screen patients for protocol eligibility, present trial concepts, and participate in informed consent processes.

Responsibilities include coordinating data collection, maintaining source documents, and reporting to sponsors. The role requires collaboration with physicians and IRB to ensure GCP and HIPAA compliance.

Qualifikationen

• Requires completion of High School Diploma or GED; Bachelor's degree preferred in Science, Sociology or related field.
• 2+ years Clinical research experience preferred.
• Familiarity with FDA/IRB regulations and GCP guidelines.

Aufgaben

• Coordinate independent study activities including screening patients for protocol eligibility.
• Schedule patients for research visits and procedures.
• Document changes in patient condition and protocol adherence on Case Report Forms (CRFs).
• Maintain accurate source documents for all research procedures.
• Collect, document, and report data; respond to sponsor queries promptly.

Kenntnisse

Study coordination

Patient screening

Informed consent

Data collection

Documentation

Regulatory compliance

IRB liaison

HIPAA compliance

GCP guidelines

Ausbildung

High School Diploma/GED

Bachelor's Degree in Science or related

Sociology or related degree

Jobbeschreibung

Cedars-Sinai in Los Angeles is hiring a Clinical Research Coordinator II for a hybrid role requiring four on-site days per week. The coordinator will screen patients for protocol eligibility, present trial concepts, and participate in informed consent processes.

Responsibilities include coordinating data collection, maintaining source documents, and reporting to sponsors. The role requires collaboration with physicians and IRB to ensure GCP and HIPAA compliance.