Clinical Research Associate

Piper Companies is seeking a Clinical Research Associate (CRA) to support a leading organization within the clinical research industry across the United States. The Clinical Research Associate (CRA) will provide site management and monitoring support for clinical trials within Oncology, Cardiovascular, GLP-1/Obesity, Diabetes, or Ophthalmology research programs. Multiple openings are available, and candidates may specialize in one or more therapeutic areas.

Responsibilities of the Clinical Research Associate (CRA): Conduct onsite and remote monitoring activities to evaluate study progress, participant safety, and protocol compliance. Lead site activation efforts, including investigator training and study start-up readiness assessments. Review clinical data, source documentation, and regulatory records to ensure accuracy and completeness. Partner with investigative sites and internal study teams to address findings, resolve issues, and maintain study timelines. Support ongoing oversight of clinical trials through routine travel, monitoring visits, and site relationship management.

Qualifications of the Clinical Research Associate (CRA): Bachelors degree in Life Sciences, Nursing, Healthcare, or a related scientific field. 2+ years of clinical monitoring experience within a pharmaceutical, biotechnology, CRO, or clinical research environment. Experience supporting studies in Oncology, Cardiovascular, GLP-1/Obesity, Diabetes, Ophthalmology, or other related therapeutic areas. Experience in all therapeutic areas is not required. Working knowledge of EDC platforms, CTMS applications, and clinical trial technologies. Strong understanding of ICH-GCP guidelines, regulatory requirements, and clinical research best practices with excellent communication and organizational skills.

Compensation of the Clinical Research Associate (CRA): Salary Range: $100,000 - $140,000 dependent on experience Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

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, Clinical Monitoring, Site Monitoring, Site Management, CRO, Biotechnology, Pharmaceutical Research, Oncology Research, Cardiovascular Research, Diabetes Research, GLP-1 Studies, Obesity Research, Ophthalmology Research, Clinical Operations, EDC Systems, CTMS, GCP, ICH Guidelines, FDA Regulations, Study Start-Up, Site Initiation Visits, Interim Monitoring Visits, Closeout Visits, Source Data Verification, Data Integrity, Protocol Compliance, Regulatory Compliance, Clinical Development, Trial Management, Investigator Relations, Multi-Site Studies, Patient Safety, Risk-Based Monitoring, Clinical Documentation, Drug Development, Research Compliance, Clinical Systems, Study Oversight