Piper Companies is seeking a detail-oriented and highly organized Clinical Research Associate (CRA) to support the planning, execution, monitoring, and closeout of clinical trials. The CRA is a traveling-based role - Southeast & Northeast regions.

Responsibilities of the CRA:

• Conduct site qualification, initiation, routine monitoring, and closeout visits for clinical research studies
• Ensure clinical trials are conducted according to study protocols, GCP guidelines, FDA regulations, and applicable local requirements
• Review source documentation, informed consent forms, and regulatory documents for accuracy and compliance
• Monitor patient recruitment, enrollment, retention, and protocol compliance
• Maintain accurate monitoring reports and study documentation within required
• Assist with study start-up activities, including regulatory submissions and site training
• Support audit and inspection readiness activities
• Track study milestones and provide regular updates on site performance and study progress

Qualifications of the CRA:

• 4+ years of clinical research experience, preferably as a Clinical Research Associate or on-site monitoring
• CRA certification (ACRP, SOCRA, or equivalent)
• Experience in oncology, immunology, cardiology, neuroscience, or rare disease studies.
• Experience working with electronic data capture (EDC) systems
• Familiarity with risk-based monitoring methodologies
• Knowledge of ICH-GCP guidelines, FDA regulations, and clinical trial processes
• Experience monitoring Phase I-IV clinical trials preferred.
• Proficiency with Microsoft Office Suite and Clinical Trial Management Systems (CTMS)
• Ability to travel up to 50% as required
• Bachelor''s degree in Life Sciences, Biology, Nursing, Public Health, or a related field

Compensation for the Clinical Research Associate:

• Salary: $110,000 - $140,000 based on years of relevant experience
• Comprehensive Benefits: Medical, Dental, Vision, 401k, Sick leave required as by law, PTO, Holidays

This job opens for applications on 7/14/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords:

Clinical Research Associate, CRA, Clinical Trial, Phase I, Phase II, Phase III, Phase IV, on-site monitoring, risk-based monitoring, clinical research, GCP, CTMS, Clinical Trial Management System, Oncology, Cardiology, Diabetes, Immunology, Ophthalmology, Neuroscience, Neuro, EDC, Electronic Data Capture, ICF, Informed Consent Form, CRF, Case Report Form, ACRP, SOCRA, Clinical Trial Associate, Clinical Operations, Study Monitoring, Study Timeline, Study Management, Site Management, SQV, Site Qualification Visit, SIV, Site initiation Visit, Interim Monitoring Visit, IMV, Principal Investigator, Closeout, Trial Master File, TMF, ICH-GCP, FDA, EMA, Regulatory Compliance, SOP, IRB, SDV, Source Data Verification, RBM, Study Documentation, Query Resolution, Data Reconciliation, Source Document, CRO, Clinical Research Organization, AE, Adverse Event, SAE, Serious Adverse Event, Pharmacovigilance, Patient Safety Monitoring, Medidata, RAVE, Rare Disease, Veeva, Trial Interactive, Oracle, Florence, REDCap

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Skills:
Biology, Cardiology, Clinical Information Systems, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Clinical Trial Management, Detail Oriented, Disease Investigation, Electronic Data Capture (EDC), FDA Requirements, GCP (Good Clinical Practices), ICH Regulations, Immunology, Legal, Microsoft Office, Neuroscience, Nursing, Oncology, Organizational Skills, Performance Analysis, Phase I Clinical Trials, Phase IV Clinical Trials, Public Health, Regulatory Submissions, Risk Management, Society of Clinical Research Associates (SoCRA), Startup, Willing to Travel

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Zp Group Llc