Onsite Oncology Clinical Research Coordinator

The US Oncology Network; Winchester (VA); On-site; USD 73,000 - 84,000; Full time

Job summary

Shenandoah Oncology in Winchester, VA is seeking a detail‑oriented Clinical Research Coordinator to manage clinical trials and support patients throughout their research journey. This is a Full‑Time Onsite role, Monday–Friday, aligned with The US Oncology Network.

Ideal candidates will thrive in a fast‑paced healthcare environment, ensure protocol compliance, obtain informed consent, document findings, and collaborate with providers, monitors, and researchers to advance cancer treatment.

Qualifications

• Associate's degree in a clinical or scientific discipline required, or an equivalent combination of education, clinical research experience, and applicable certification.
• Minimum three years of Clinical Research Coordinator experience in a clinical research setting.
• SoCRA (CCRP) or ACRP certification preferred.

Responsibilities

• Screen potential participants for protocol eligibility.
• Present trial concepts and details, obtain informed consent, and enroll participants into clinical trials.
• Coordinate participant care in compliance with protocol requirements.
• May disburse investigational product and maintain accountability records.
• Oversee preparation of provider orders to ensure protocol compliance.
• Maintain regulatory documents per SOPs and regulations.
• May assist with scheduling monitoring and auditing visits and interact with monitors/auditors.

Skills

Informed consent process

Regulatory documentation

Participant scheduling

Study monitoring support

Data collection & reporting

Education

Associate's degree in clinical or scientific discipline

Bachelor's degree preferred

Tools

SoCRA/ACRP certification

Job description

Shenandoah Oncology in Winchester, VA is seeking a detail‑oriented Clinical Research Coordinator to manage clinical trials and support patients throughout their research journey. This is a Full‑Time Onsite role, Monday–Friday, aligned with The US Oncology Network.

Ideal candidates will thrive in a fast‑paced healthcare environment, ensure protocol compliance, obtain informed consent, document findings, and collaborate with providers, monitors, and researchers to advance cancer treatment.