Onsite Cancer Research Coordinator - Impactful Trials

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

Job summary

Shenandoah Oncology is seeking a detail-oriented Clinical Research Coordinator to manage clinical trials and support patients throughout their research journey. This full-time, onsite position emphasizes patient care, accuracy, and compliance within a fast-paced healthcare setting.

The role involves screening participants, enrolling with informed consent, coordinating visits, and maintaining regulatory documentation, with potential involvement in inventory, scheduling, and collaboration with

Qualifications

• Associate degree or higher in clinical/scientific field or equivalent experience.
• Minimum three years of Clinical Research Coordinator experience in a U.S. setting; oncology experience preferred.
• SoCRA/ACRP certification preferred.

Responsibilities

• Screen potential participants for protocol eligibility.
• Present trial concepts to participants and enroll in trials with informed consent.
• Coordinate participant care to ensure protocol compliance and data integrity.
• Maintain regulatory documents and assist with billing guides as needed.
• Prepare study documentation and assist with audits/monitors.

Skills

Participant screening

Informed consent

Regulatory documentation

Study coordination

Data collection

Education

Associate's degree

Bachelor's degree preferred

Job description

Shenandoah Oncology is seeking a detail-oriented Clinical Research Coordinator to manage clinical trials and support patients throughout their research journey. This full-time, onsite position emphasizes patient care, accuracy, and compliance within a fast-paced healthcare setting.

The role involves screening participants, enrolling with informed consent, coordinating visits, and maintaining regulatory documentation, with potential involvement in inventory, scheduling, and collaboration with