Clinical Research Coordinator II: Endocrinology Trials

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

Job summary

Cedars-Sinai in Los Angeles is seeking a Clinical Research Coordinator II to support the Endocrinology Division in the Department of Medicine. You will coordinate patient screening, consent, data collection, and reporting while ensuring regulatory compliance and high-quality documentation.

Responsibilities include CRF data entry, coordinating monitoring visits, and collaborating with the IRB and regulatory staff to handle adverse events and protocol deviations, all while upholding GCP and HIPAA

Qualifications

• 2 years of clinical research experience is required.
• ACRP/SOCRA certification is preferred.
• Bachelor's degree in a Science, Sociology, or related field is preferred.
• High School Diploma/GED is required.

Responsibilities

• Schedules patients for research visits and procedures.
• Documents thoroughly on Case Report Forms (CRFs).
• Maintains accurate source documents related to research procedures.
• Schedules and participates in monitoring and auditing activities.
• Notifies supervisor about data quality and study conduct concerns.
• Coordinates with IRB on adverse events and protocol deviations.
• Maintains research practices using Good Clinical Practice (GCP) guidelines.
• Ensures HIPAA confidentiality.

Education

High School Diploma/GED

Bachelor's degree in a Science, Sociology, or related field

ACRP/SOCRA certification

Job description

Cedars-Sinai in Los Angeles is seeking a Clinical Research Coordinator II to support the Endocrinology Division in the Department of Medicine. You will coordinate patient screening, consent, data collection, and reporting while ensuring regulatory compliance and high-quality documentation.

Responsibilities include CRF data entry, coordinating monitoring visits, and collaborating with the IRB and regulatory staff to handle adverse events and protocol deviations, all while upholding GCP and HIPAA