Piper Companies is seeking an Oncology Clinical Research Associate to support a leading organization within the clinical trials industry in The United States. 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 - $140,000 • Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays This job opens for applications on 9/4/26. Applications for this job will be accepted for at least 30 days from the posting date. #LI-HB1 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