Remote Clinical Trials Data Specialist

City of Hope; United States; Remote; USD 65,000 - 90,000; Full time

Job summary

City of Hope is seeking a Clinical Trials Data Coordinator to join our remote team. In this role, you will ensure data integrity across studies, perform data abstraction, CRF completion, and query resolution, and coordinate sponsor monitor visits to keep data audit-ready.

You will oversee electronic research records in the CTMS and handle patient information with strict HIPAA compliance, working closely with the clinical research team to communicate deviations and ensure protocol adherence.

Qualifications

• Bachelor's Degree or equivalent; relevant oncology trial experience preferred.
• At least two years of experience in oncology clinical trials.
• Working knowledge of clinical trial regulations and IRB requirements.

Responsibilities

• Ensure data integrity for various research studies.
• Perform data abstraction, CRF completion, and query resolution.
• Coordinate sponsor monitor visits and maintain audit-ready data.
• Oversee electronic records in the CTMS and protect patient information.
• Collaborate with the clinical research team and communicate protocol deviations clearly.

Skills

GCP knowledge

FDA regulations

NIH guidelines

HIPPA regulations

Education

Bachelor's Degree

Job description

City of Hope is seeking a Clinical Trials Data Coordinator to join our remote team. In this role, you will ensure data integrity across studies, perform data abstraction, CRF completion, and query resolution, and coordinate sponsor monitor visits to keep data audit-ready.

You will oversee electronic research records in the CTMS and handle patient information with strict HIPAA compliance, working closely with the clinical research team to communicate deviations and ensure protocol adherence.