• Drive the execution of PV compliance activities to meet global regulatory requirements (DEA, State Board of Pharmacy, URAC and ACHC, OIG, etc.) and industry standards, with a focus on operational integration with Quality Assurance and Patient Solutions. • Partner closely with Quality Assurance and Operations to develop, implement, and manage PV compliance frameworks, including SOPs, processes, and systems for program drug safety reporting. • Work directly with cross-functional teams, including Patient Solutions, Pharmacy, Regulatory Affairs, and Clinical, to facilitate an integrated and patient-centered approach to PV compliance. • Ensure PV systems are audit-ready, including preparing for and supporting regulatory authority inspections. • Conduct regular assessments of PV risk management, identify and address compliance gaps, and recommend improvements in collaboration with QA and Patient Solutions. • Monitor regulatory changes in PV and assess their impact on front-end operations, keeping stakeholders informed of updates and required actions. • Oversee and assess quality performance of internal and external resources, regularly reporting to senior management. • Support internal and external PV audits, including audits of business partners and service providers, ensuring findings are communicated and addressed. • Contribute to the development and delivery of PV compliance training tailored to frontline and patient solutions teams. • Facilitate the timely preparation and submission of regulatory filings related to PV, including safety reports and risk management plans. • Assist in investigations of compliance breaches, implementing corrective and preventive actions (CAPAs) as needed. • Actively engage in continuous improvement initiatives to enhance PV processes and ensure quality integration across all frontline operations. • Performs other related duties as assigned by management.