Piper Companies is seeking an Oncology Clinical Research Associate to support a leading organization within the clinical trials industry in Chicago, IL. The Oncology Clinical Research Associate will play a vital role in managing investigative sites and ensuring the successful delivery of clinical studies across a national footprint, with an emphasis on high-quality data and regulatory compliance.

Responsibilities of the Oncology Clinical Research Associate:
• Perform site monitoring activities through both remote evaluations and on-location visits to ensure study integrity
• Lead site initiation efforts, confirming preparedness and compliance prior to study launch
• Assess site performance, reviewing data accuracy and adherence to protocols and regulatory standards
• Contribute to the development and refinement of study documentation, tools, and operational processes
• Maintain consistent communication with study teams and travel as required to support site oversight

Qualifications of the Oncology Clinical Research Associate:
• 2–4 years of experience conducting monitoring activities within clinical research settings
• Practical experience working with electronic data capture (EDC) systems and clinical trial technologies
• Oncology research exposure is a significant advantage
• Strong organizational capabilities with the ability to manage multiple sites and competing priorities
• Effective communication and analytical skills within a regulated clinical environment

Compensation of the Oncology Clinical Research Associate:
• Salary Range: $100,000 - $120,000
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 7/2/26. Applications for this job will be accepted for at least 30 days from the posting date.

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Keywords: Clinical Research Associate, CRA, Clinical Trials, Site Monitoring, EDC Systems, Oncology Research, GCP, ICH Guidelines, Study Start-Up, Remote Monitoring, On-site Monitoring, Clinical Operations, Protocol Compliance, Data Review, Regulatory Oversight, CRO, Clinical Development, Trial Management, Multi-site Studies, Investigator Relations, Monitoring Visits, Risk-Based Monitoring, Clinical Documentation, Pharma Research, Biotech Studies, Data Integrity, Study Activation, Research Compliance, Trial Oversight, Drug Development, Clinical Systems