Remote Oncology Trials Data Coordinator

Mobile; Duarte (CA); Remote; USD 42,000 - 65,000; Full time

Job summary

City of Hope is seeking a Clinical Trials Data Coordinator to join a remote team supporting oncology studies. You will ensure data integrity, perform data abstraction, complete CRFs, resolve queries, and coordinate sponsor monitor visits, maintaining audit-ready records in the CTMS.

Ideal candidates will have strong knowledge of GCP, FDA regulations, NIH guidelines, and HIPAA, plus excellent communication and meticulous attention to detail to ensure protocol adherence and timely study execution.

Qualifications

• Bachelor’s Degree, relevant experience may substitute for degree.
• At least two years of experience related to the conduct of oncology clinical trials.
• Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.

Responsibilities

• Data abstraction and CRF completion as part of study workflow.
• Query resolution and sponsor monitor visit coordination.
• Oversight of electronic research records and CTMS data.
• Maintaining audit-ready data and study parameters per protocol.
• Communicate protocol deviations and issues clearly and timely.

Skills

GCP knowledge

FDA regulations

NIH guidelines

HIPAA regulations

Communication skills

Deadline-driven

Detail-oriented

Education

Bachelor’s Degree

Tools

CTMS

Job description

City of Hope is seeking a Clinical Trials Data Coordinator to join a remote team supporting oncology studies. You will ensure data integrity, perform data abstraction, complete CRFs, resolve queries, and coordinate sponsor monitor visits, maintaining audit-ready records in the CTMS.

Ideal candidates will have strong knowledge of GCP, FDA regulations, NIH guidelines, and HIPAA, plus excellent communication and meticulous attention to detail to ensure protocol adherence and timely study execution.