Licensed healthcare professional with 16+ years of experience in patient care, clinical operations, and regulatory compliance. Proven ability to manage treatment protocols, document health outcomes, and ensure adherence to ethical and procedural standards in fast-paced clinical settings. Skilled in patient intake, informed consent communication, EHR documentation, and workflow coordination. Known for precision, confidentiality, and a collaborative work ethic. Eager to transition into human subject research to support participant screening, protocol implementation, and accurate data collection within regulated research environments.