Oncology Trials Coordinator II - PRN

COOPER PEDIATRICS; Camden (NJ); On-site; USD 52,000 - 70,000; Full time

Job summary

Cooper University Health Care in New Jersey seeks an Oncology Research Coordinator I to provide oversight of oncology clinical studies, focusing on Quality of Life and specimen trials, while supporting study start-up and regulatory processes.

This entry-level role collaborates with sponsors, IRB, and Regulatory/Operations teams to maintain regulatory binders, track documentation, and coordinate site visits and audits.

Qualifications

• 3-5 Related experience
• Bachelor Degree Preferred

Responsibilities

• Oversight of oncology clinical studies, managing Quality of Life and specimen trials.
• Learning and progressing to manage oncology treatment trials.
• Work with sponsors during study start-up to prepare regulatory documents and maintain study binders.
• Coordinate IRB submissions, amendments, continuing reviews, and adverse event reports.
• Provide updates to Regulatory and Operations teams on study status.
• Maintain delegation of authority logs and ensure staff training on protocols.
• Coordinate site initiation visits, monitoring visits, and close-out visits; prepare post-visit documents.
• Maintain tracking for protocol paperwork and coordinate FDA submissions and audits.

Education

Bachelor degree preferred

Job description

Cooper University Health Care in New Jersey seeks an Oncology Research Coordinator I to provide oversight of oncology clinical studies, focusing on Quality of Life and specimen trials, while supporting study start-up and regulatory processes.

This entry-level role collaborates with sponsors, IRB, and Regulatory/Operations teams to maintain regulatory binders, track documentation, and coordinate site visits and audits.