Clinical Research Coordinator I — Kidney Transplant Trials

Cedars-Sinai; Los Angeles (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

Cedars-Sinai in Los Angeles is seeking a Clinical Research Coordinator I to work independently on study coordination, patient screening for protocol eligibility, and contributing to informed consent processes. You will ensure accurate source documents, data collection, entry and timely sponsor communications in a fast-paced transplant research setting.

Responsibilities include scheduling visits, documenting events on CRFs, coordinating monitoring visits, and maintaining HIPAA and GCP compliance

Qualifications

• High School Diploma or GED required.
• Bachelor's Degree in Science, Sociology or related field preferred.
• 1 year clinical research related experience required.

Responsibilities

• Coordinate studies independently, screen patients for eligibility, and participate in informed consent.
• Collect, document, and report study data and source documents in a timely manner.
• Schedule visits, monitor visits, site initiation visits, close-out visits, and audits.
• Communicate with sponsors regarding protocol clarifications and adverse events.
• Maintain compliance with FDA, IRB, HIPAA and GCP guidelines.

Education

High School Diploma/GED, required

Bachelor's Degree, Science, Sociology or related degree, preferred

Job description

Cedars-Sinai in Los Angeles is seeking a Clinical Research Coordinator I to work independently on study coordination, patient screening for protocol eligibility, and contributing to informed consent processes. You will ensure accurate source documents, data collection, entry and timely sponsor communications in a fast-paced transplant research setting.

Responsibilities include scheduling visits, documenting events on CRFs, coordinating monitoring visits, and maintaining HIPAA and GCP compliance