Oncology Clinical Trials Regulatory Coordinator

Halifaxhealth; Daytona Beach (FL); On-site; USD 60,000 - 90,000; Full time

Job summary

Qualifications

• Minimum 2 years’ experience in a clinical trial role, oncology experience preferred.
• CPR Training
• Regulatory knowledge and experience with IRB, FDA, and GCP guidelines preferred.
• Experience with databases and Microsoft Office (Excel/Word).
• Ability to manage multiple priorities and work independently.

Responsibilities

• Coordinate regulatory compliance for clinical trials and ensure IRB and sponsor requirements are met.
• Assist with identifying potential trial participants and obtaining informed consent.
• Enter and manage data in trial databases; ensure data accuracy and timely submissions.
• Support investigators with protocol entry, adherence to compliance, and follow-up activities.
• Attend tumor boards and interdepartmental meetings as needed.

Skills

Databases experience

Patient data handling

Excel

Word

Time management

Good Clinical Practice

Clinical research certification

Education

Clinical Trial regulatory certification

CPR Certification

SOCRA/ACRP/ONS certification

Tools

Microsoft Office

Job description