Oncology Clinical Research Coordinator - Data & Compliance

City of Hope; Duarte (CA); Hybrid; USD 75,000 - 95,000; Full time

Job summary

City of Hope in Duarte, CA seeks a Clinical Research Coordinator to maintain data integrity across multiple oncology trials. You will abstract data, complete CRFs, and ensure timely queries while coordinating sponsor visits and audits within CTMS and regulatory frameworks.

The role requires a Bachelor’s degree and 2+ years in oncology trials, with strong GCP, FDA, NIH, and HIPAA knowledge; you will work as part of a collaborative clinical research team across disease units.

Qualifications

• Bachelor’s degree required; experience can substitute.
• At least 2 years of oncology clinical trials experience in an academic setting.
• Strong knowledge of GCP, FDA regulations, NIH guidelines, and HIPAA.

Responsibilities

• Order and complete protocol-required procedures including biospecimen handling.
• Abstract source data, complete paper/eCRFs, resolve data queries.
• Maintain audit-ready studies per GCP and regulatory requirements.
• Coordinate study meetings, monitoring visits, audits, and data verification.

Skills

Data management

Attention to detail

Communication skills

Education

Bachelor’s Degree

Tools

CTMS

IRB systems

Job description

City of Hope in Duarte, CA seeks a Clinical Research Coordinator to maintain data integrity across multiple oncology trials. You will abstract data, complete CRFs, and ensure timely queries while coordinating sponsor visits and audits within CTMS and regulatory frameworks.

The role requires a Bachelor’s degree and 2+ years in oncology trials, with strong GCP, FDA, NIH, and HIPAA knowledge; you will work as part of a collaborative clinical research team across disease units.