Oncology Clinical Research Coordinator

US Oncology Inc.; Mobile (AL); On-site; USD 52,000 - 76,000; Full time

Job summary

Southern Cancer Center seeks a Clinical Research Coordinator to coordinate patient screening, enrollment, and data collection for oncology trials. You will ensure regulatory compliance, maintain study records, and assist with investigational drug management.

You will work with physicians, sponsors, and monitors in a fast-paced oncology setting, ensuring accurate data and patient safety across studies.

Qualifications

• Associate degree in a clinical, scientific, or healthcare-related field is required.
• Bachelor’s degree preferred.
• Minimum of one year of experience in a clinical or scientific healthcare setting is required.
• Oncology experience strongly preferred.
• Experience working with physicians preferred.
• Proficiency in Microsoft Office applications required.

Responsibilities

• Coordinate patient screening, enrollment, data collection, and monitoring for clinical trials.
• Ensure regulatory compliance with FDA, GCP, and USOR SOPs.
• Maintain regulatory documents and study records.
• Assist with investigational drug management and accountability.
• Collaborate with physicians, sponsors, monitors, and auditors.
• Support patient confidentiality and professional conduct.

Skills

Verbal and written communication

Organization and prioritization

Time management

Independent and collaborative work

Clinical data monitoring

Microsoft Office

Education

Associate degree in clinical/science/healthcare field

Bachelor’s degree preferred

Tools

Microsoft Office

Job description

Southern Cancer Center seeks a Clinical Research Coordinator to coordinate patient screening, enrollment, and data collection for oncology trials. You will ensure regulatory compliance, maintain study records, and assist with investigational drug management.

You will work with physicians, sponsors, and monitors in a fast-paced oncology setting, ensuring accurate data and patient safety across studies.