Oncology Clinical Research Coordinator - Patient-Focused Trials

US Oncology Inc.; 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 role runs Monday–Friday and involves screening participants, coordinating care, and ensuring protocol compliance.

This position offers an opportunity to contribute to cutting-edge cancer research within The US Oncology Network, with a focus on accurate data collection, regulatory adherence, and collaborative

Responsibilities

• Screens potential participants for protocol eligibility.
• Presents trial concepts and details to participants, participates in the informed consent process, and enrolls participants into clinical trials.
• Coordinates participant care in compliance with protocol requirements.
• May disburse investigational product and maintain accountability records.
• Oversees preparation of orders by providers to ensure protocol compliance.
• Packages and ships laboratory specimens to central vendors as applicable.
• Completion of Hazmat and/or IATA training may be required.
• In collaboration with providers, reviews participants for changes in condition, adverse events, concomitant medications, protocol compliance, and response to study treatment.
• Thoroughly document all findings and participate in data collection.
• Prepares study-related documentation, including protocol worksheets, adverse event reports, institutional review board (IRB) documents, and annual continuing review reports.
• Maintains regulatory documents in accordance with organizational SOPs and applicable regulations.
• May assist with scheduling monitoring and auditing visits and interact with monitors/auditors as needed.
• May collaborate with research leadership in study selection processes.

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 role runs Monday–Friday and involves screening participants, coordinating care, and ensuring protocol compliance.

This position offers an opportunity to contribute to cutting-edge cancer research within The US Oncology Network, with a focus on accurate data collection, regulatory adherence, and collaborative