Oncology Clinical Research Coordinator - Patient Trials

US Oncology Inc.; Arlington (VA); On-site; USD 60,000 - 90,000; Full time

Job summary

Virginia Cancer Specialists, an affiliate of US Oncology, is seeking a Full Time Clinical Research Coordinator for our Arlington office. A Bachelor’s degree in a clinical or scientific field is preferred, with oncology experience desirable.

The coordinator will screen, enroll, and monitor patients on clinical trials, ensuring protocol compliance and accurate data entry. Responsibilities include consent, billing reviews, education of staff and patients, and collaboration with physicians to manage

Qualifications

• Education: Associate's degree required; Bachelor's preferred.
• Experience: minimum three years in a clinical or scientific field, oncology preferred.
• Certification: SOCRA or ACRP certification preferred.

Responsibilities

• Coordinate screening, enrollment, and maintenance of patients on clinical trials.
• Ensure protocol compliance and assist with consent process.
• Document data accurately and timely; maintain regulatory documents.
• Assist with education and training of staff and patients.
• Support billing per protocol and recruitment strategies.
• Communicate with physicians about study requirements and adverse events.
• Schedule monitoring and liaise with monitors/auditors as needed.
• Perform patient assessments and administer orders to assure protocol adherence.

Skills

Excellent communication skills

Excellent organizational skills

Time management

Multi-tasking

Interpersonal skills

Attention to detail

Education

Bachelor's degree in a clinical or scientific related discipline

Associate's degree in a clinical or scientific related discipline

Tools

Microsoft Office

Job description

Virginia Cancer Specialists, an affiliate of US Oncology, is seeking a Full Time Clinical Research Coordinator for our Arlington office. A Bachelor’s degree in a clinical or scientific field is preferred, with oncology experience desirable.

The coordinator will screen, enroll, and monitor patients on clinical trials, ensuring protocol compliance and accurate data entry. Responsibilities include consent, billing reviews, education of staff and patients, and collaboration with physicians to manage