$125,000–$150,000 Per Year
Adverse Events, Best Practices, Clinical Data, Clinical Data Management, Clinical Research, Clinical Trial, Contract Research Organization (CRO), Cross-Functional, Data Quality, Documentation, Electronic Data Capture (EDC), FDA Requirements, GCP (Good Clinical Practices), ICH Regulations, Industry Standards, Keyword Research, Legal, Maintain Compliance, Oncology, Problem Solving Skills, Regulations, Safety Process, Site Evaluation, Startup, System Operations
Piper Companies is seeking a Clinical Research Associate (CRA) to join a leading organization within the clinical research industry for a permanent position based in Chicago, Illinois. The Clinical Research Associate (CRA) will play a key role in overseeing oncology-focused studies across multiple sites, ensuring trial execution aligns with regulatory expectations and study requirements.
Responsibilities of the Clinical Research Associate
- Perform site visits both in-person and remotely, including study initiation, routine monitoring, and close-out activities
- Ensure investigative sites follow protocol guidelines, regulatory standards, and industry best practices throughout oncology trials
- Evaluate clinical data for accuracy and completeness, including safety events and key study outcomes
- Assist with study start-up efforts such as site assessments, regulatory documentation, and activation
processes
- Partner with cross-functional teams and site personnel to provide updates on study progress, risks, and issue resolution
Requirements of the Clinical Research Associate
- 3-5 years of experience in a CRA role with hands-on site monitoring responsibilities
- Direct involvement in oncology clinical trials with knowledge of relevant endpoints and safety reporting processes
- Experience working with EDC systems and clinical trial technology platforms
Compensation for the Clinical Research Associate
- Salary Range: $125,000 - $150,000
- Comprehensive Benefits: Medical, Dental, Vision, 401(k), Paid Time Off, Sick Leave (as required by law), and Paid Holidays
This job opens for applications on 6/26/26. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: clinical research, oncology trials, monitoring, GCP, regulatory compliance, site management, clinical data review, adverse events, safety reporting, EDC systems, clinical operations, study start-up, protocol adherence, FDA regulations, ICH guidelines, data integrity, stakeholder communication, CRO, site visits, trial oversight
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