Hybrid Oncology Research Nurse/Coordinator

US Oncology Network-wide Career Opportunities; Norfolk (VA); Hybrid; USD 48,000 - 129,000; Full time

Benefits offered by this job

Medical/Dental/Vision

Life Insurance

401(k)

Job summary

Virginia Oncology Associates in Norfolk is seeking a Clinical Research Coordinator or Clinical Research RN to join our oncology practice.

This full-time, hybrid position features a compensation range of $47,964.80 to $128,939.20, with duties including patient screening for protocol eligibility, informed consent, enrollment, care coordination, and collaboration with sponsors to maintain protocol compliance; most tasks are computer-based. Strong communication and data-entry skills are essential.

Qualifications

• Associates degree in a clinical or scientific discipline required.
• Experience in clinical research preferred.
• Experience with computer data entry and database management.
• Excellent written and oral communication skills.
• Ability to read, analyze, and interpret protocols and regulatory documents.

Responsibilities

• Screen potential patients for protocol eligibility and present trial concepts to patients.
• Participate in informed consent process and enroll patients on protocol.
• 75% of the job is computer-based and direct patient care is limited.
• Coordinate patient care in compliance with protocol requirements.
• Work directly with other research bases and sponsors.
• Oversee preparation of physician orders to ensure protocol compliance.
• Communicate with physicians regarding study requirements, dose modifications and adverse event reporting.

Skills

Data entry

Database management

Communication skills

Education

Associate degree in clinical or scientific discipline

BSN preferred

Job description

Virginia Oncology Associates in Norfolk is seeking a Clinical Research Coordinator or Clinical Research RN to join our oncology practice.

This full-time, hybrid position features a compensation range of $47,964.80 to $128,939.20, with duties including patient screening for protocol eligibility, informed consent, enrollment, care coordination, and collaboration with sponsors to maintain protocol compliance; most tasks are computer-based. Strong communication and data-entry skills are essential.