Oncology CRA - Lead Multi-Site Monitoring

Piper Companies; United States; On-site; USD 100,000 - 140,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401K

PTO

Sick Leave

Holidays

Job summary

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.

The role involves site monitoring (remote and on-site), initiation, data review, and

Qualifications

• 2–4 years of experience conducting monitoring activities in clinical research.
• Hands-on experience with EDC systems and trial technologies.
• Exposure to oncology research is advantageous.
• Strong organizational and multi-site management skills.
• Effective communication within a regulated clinical environment.

Responsibilities

• Perform site monitoring through remote evaluations and on-site visits.
• Lead site initiation and ensure readiness prior to study launch.
• Assess site performance and data accuracy per protocols and standards.
• Contribute to study documentation and process improvements.
• Maintain ongoing communication with study teams and travel as needed.

Skills

Site monitoring

Regulatory compliance

Data review

Project coordination

Communication

Tools

EDC systems

Job description

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.

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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