Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry for a remote permanent role with 60-75% travel across the United States. This CRA II will support cardiovascular, CNS, and metabolic studies while partnering closely with investigative sites to ensure high-quality trial execution. Responsibilities of the Clinical Research Associate II include: · Perform routine and close-out monitoring visits to ensure studies are conducted in alignment with GCP, ICH, and applicable regulations. · Serve as the primary point of contact for assigned research sites, fostering strong relationships and ongoing communication. · Review site data, source documentation, and regulatory files to confirm accuracy, completeness, and protocol adherence. · Provide guidance and training to site staff on protocol requirements, study procedures, and compliance expectations. · Identify, document, and escalate quality or compliance concerns while supporting resolution efforts. Qualifications for the Clinical Research Associate II include: · 1–4 years of onsite clinical monitoring experience, aligned to CRA II or Senior CRA I level. · Experience supporting clinical trials within cardiovascular, CNS, diabetes, or metabolic indications. · Strong working knowledge of GCP, ICH guidelines, and FDA regulatory requirements. · Proficiency with CTMS, EDC systems, and standard clinical trial documentation. · Bachelor’s degree in life sciences, nursing, or a related discipline; Spanish fluency is highly preferred for candidates based in Florida or Puerto Rico. Compensation for the Clinical Research Associate II: Salary Range: $100,000–$125,000/year (USD) Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401(k) This job opens for applications on 10/2/26. Applications for this job will be accepted for at least 30 days from the posting date. Keywords: clinical research, clinical trials, CRA, GCP, ICH, regulatory compliance, site monitoring, clinical monitoring, CTMS, EDC, cardiovascular studies, CNS trials, diabetes research, GLP-1, site management, FDA regulations, clinical operations, documentation, quality assurance, protocol compliance, investigator sites, patient safety, clinical development. #LI-MB1 #LI-REMOTE