Vice President, U.S. Compliance

Base pay range

$/yr - $/yr

Additional compensation types

Annual Bonus and RSUs

The Vice President, U.S. Compliance will support Rev Med’s U.S. business. This role will lead the strategy, development, and execution of the company’s U.S. healthcare compliance program, ensuring all activities are conducted ethically and in accordance with applicable laws, regulations, and industry codes. This executive will be instrumental in shaping and sustaining a culture of integrity as the company advances and commercializes its oncology pipeline.

This position reports to the Vice President, Compliance.

• Design, implement, and continuously improve a comprehensive U.S. healthcare compliance program consistent with OIG Guidance, PhRMA Code, and applicable industry standards
• Establish and maintain policies, procedures, and systems to ensure compliant operations across all U.S. commercial, medical, and research activities
• Provide regular compliance updates to executive leadership, including risk assessments, metrics, and remediation plans
• Serve as the company’s U.S. Compliance Officer and key representative in interactions with regulators, external counsel, and industry associations
• Coordinate compliance guidance and initiatives with ex‑US compliance teams

• Partner closely with the Healthcare Law team to ensure consistency between legal interpretation and compliance operations
• Maintain a clear functional separation of responsibilities between Compliance and Healthcare Law
• Collaborate to deliver integrated, practical guidance to internal clients—particularly within Commercial, Medical Affairs, Clinical Development, and Market Access functions

• Provide compliance leadership for all U.S. programs, including those involving targeted therapies, precision medicine, and molecular diagnostics
• Oversee compliance in complex scientific collaborations—including investigator‑sponsored trials (ISTs), research collaborations, and co‑promotion or data‑sharing arrangements
• Ensure compliant governance of interactions with oncology healthcare professionals (HCPs), key opinion leaders (KOLs), and academic research centers
• Oversee U.S. aggregate spend, transparency, and Sunshine Act reporting obligations, including oncology‑specific speaker programs, congress sponsor ships, and advisory boards
• Provide compliance support for patient access programs, patient support services, and specialty distribution channels, ensuring compliant interactions with patients, caregivers, and advocacy groups

• Develop and implement risk‑based compliance training for field and headquarters staff, tailored to oncology business activities (e.g., clinical data dissemination, compassionate use programs)
• Design and oversee monitoring and auditing plans covering commercial field conduct, grants, consulting arrangements, and medical education
• Lead investigations into potential violations, ensuring timely, thorough resolution and corrective actions
• Track, analyze, and report compliance metrics and trends to management and governance bodies

• Serve as a trusted advisor to senior leadership and cross‑functional teams on compliance risks and mitigation strategies
• Collaborate with Legal, Medical Affairs, Clinical Operations, and Market Access on compliant program design and execution
• Partner with Finance, HR, and Internal Audit to ensure unified corporate risk management
• Build, lead, mentor, and develop a team of compliance professionals committed to excellence and integrity

• J.D. from an accredited U.S. law school and member in good standing of a U.S. State Bar
• 12‑15+ years in healthcare compliance or legal roles within the biotechnology, pharmaceutical, or oncology industry
• In‑depth understanding of U.S. healthcare laws, including Anti‑Kickback Statute, False Claims Act, FDA promotional regulations, FCPA, and data privacy laws
• Proven ability to build, lead, and scale compliance programs for commercial or late‑stage clinical oncology companies
• Experience…