Oncology Clinical Trials Nurse & Coordinator

US Oncology Inc.; Roanoke (VA); On-site; USD 53,000 - 81,000; Full time

Job summary

US Oncology Research, Inc. seeks an entry-level registered nurse to coordinate screening, enrollment, and maintenance of patients on clinical trials. You will ensure protocol compliance, participate in consent, and collaborate with physicians to assess changes in condition and adverse events.

Accurate documentation and data entry are essential, along with staff education and training. The role requires current RN licensure, oncology exposure, and familiarity with GCP/regulatory standards;

Qualifications

• Current licensure as a Registered Nurse in state of practice required.
• Certification preferred: OCN, SoCRA or ACRP.
• Minimum 1 year nursing experience, preferably in oncology.
• Experience with Microsoft Office required.
• Experience in clinical research preferred.

Responsibilities

• Collaborates with physicians and providers to screen potential patients for eligibility.
• Presents trial concepts and details to patients, participates in consent, and enrolls patients.
• Coordinates patient care per protocol requirements.
• Dispenses investigational drug and provides patient teaching on administration.
• Maintains investigational drug accountability.
• Reviews patient status for changes, adverse events, and protocol compliance; documents findings.
• Reviews billing guides and submits billing information.
• Collaborates with study team on recruitment and enrollment goals.
• Promotes participant recruitment and retention in long-term trials.
• Provides clinical services and assists with regulatory document collection.

Skills

Registered Nurse

Oncology experience

Nursing experience

Clinical research

OCN certification

SoCRA certification

ACRP certification

Communication skills

Organizational skills

Education

RN license in state practice

Tools

Microsoft Office

Job description

US Oncology Research, Inc. seeks an entry-level registered nurse to coordinate screening, enrollment, and maintenance of patients on clinical trials. You will ensure protocol compliance, participate in consent, and collaborate with physicians to assess changes in condition and adverse events.

Accurate documentation and data entry are essential, along with staff education and training. The role requires current RN licensure, oncology exposure, and familiarity with GCP/regulatory standards;