Sub-Investigator - APRN/PA

Sub-Investigator (Sub-I) supports the Principal Investigator (PI) in the safe and compliant conduct of clinical trials. This role performs study-specific clinical assessments and evaluations, determines subject eligibility, provides medical care for enrolled subjects, reviews and signs off on clinical data, and ensures subject safety, rights, and well-being throughout study participation. Responsibilities include adherence to DOA, protocol, GCP, and FDA regulations; collaboration with Clinical Operations, Recruitment, QA, and Regulatory teams; and strong emphasis on data integrity and regulatory compliance. Requires MD/DO/NP/PA with active, unrestricted license; preferred prior Investigator experience; proficiency with eSource/EDC, and excellent communication skills.