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The Clinical Research Nurse Practitioner will serve as the Sub Investigator and conduct study activities as delegated by the Principal Investigator and Study Project Manager, ensuring compliance with study protocols and applicable FDA regulations. This role involves performing vital signs assessments, physical examinations, phlebotomy, and other clinical procedures as required by trial protocols. The Nurse Practitioner will also oversee study drug dispensation, monitor patient responses to treatment, and ensure precise documentation of all study-related activities. Additionally, the position requires collaboration with various stakeholders to facilitate patient recruitment and retention, as well as participation in audits and inspections to maintain data accuracy and quality.