• Lead the strategic development and execution of highly scalable regulatory programs across multiple jurisdictions, effectively communicating outcomes and insights to senior leadership. • Lead end-to-end execution of complex regulatory programs, ensuring measurable outcomes, sustainable operations, and readiness to meet evolving legal requirements while ensuring Airbnb’s obligations are met with excellence. • Translate emerging regulatory trends into actionable business strategies for senior leadership. • Partner with cross-functional technical partners to design systems and tooling that enable proactive, automated compliance solutions. • Identify and lead resolution of regulatory risks or incidents, coordinating with legal and policy counterparts to develop mitigation and escalation strategies. • Influence cross-functional roadmaps and corporate strategy through deep expertise in regulatory frameworks. • Serve as the primary liaison and operational architect for your jurisdictions, establishing operational rhythms and ensuring alignment among cross-functional stakeholders while maintaining comprehensive project documentation. • Oversee product assurance initiatives with a global perspective, ensuring meticulous attention to detail without compromising agility. • Drive high-impact strategic projects aimed at enhancing efficiency and effectiveness while also aligning with broader business goals.

• Build and sustain a high-performing team of regulatory and reference data SMEs through active coaching, clear expectations, and ongoing feedback. • Manage workload distribution, prioritization, and delivery across the team to meet regulatory milestones and Source product release commitments. • Serve as an escalation point for Source-related regulatory issues, guiding the team through complex interpretation and resolution. • Partner with Product, Engineering, and Client Success stakeholders to ensure regulatory requirements are clearly understood and operationalized in Source. • Lead, supervise, and develop a team of regulatory compliance professionals with expertise in claims pricing, reference data, and healthcare transparency requirements. • Conduct regular one-on-ones, performance reviews, and career development conversations. • Build a team culture grounded in accountability, intellectual rigor, collaboration, and continuous improvement. • Manage workload planning, capacity, and coverage to ensure consistent delivery against regulatory timelines and data release cycles. • Drive onboarding and skill development for new and existing team members as Source’s regulatory scope evolves. • Oversee the team’s monitoring, interpretation, and documentation of federal and state regulatory requirements impacting pricing, reference data and editing. • Ensure regulatory deliverables - system requirement specifications, and client-facing materials – are accurate , timely , and meet quality standards. • Manage the team’s review and disposition of regulatory changes relevant to Source across commercial, Medicare Advantage, and Medicaid lines of business. • Oversee escalation management and resolution of complex regulatory issues affecting Source customers or product functionality. • Partner with Source Product and Engineering to ensure regulatory requirements are incorporated into roadmap planning and sprint execution. • Collaborate with Client Success and Implementation teams to support health plan client inquiries related to Source regulatory content. • Represent the team’s work in cross-functional meetings, regulatory forums, and client-facing engagements as needed. • Coordinate on enterprise regulatory monitoring and cross-product impact assessments where Source data intersects with other HealthEdge platforms.

• Serve as the primary point of contact for safety and compliance with assigned service partners • Make sure service partner drivers remain compliant by conducting regular driver file audits and reviewing documentation • Verify new driver qualifications and make sure all required documentation is complete before onboarding • Conduct vehicle inspections and monitor compliance with safety standards • Visit service partners and school districts to provide on-site support and maintain strong working relationships • Meet regularly with service partners to review compliance expectations and address safety concerns • Collaborate with school districts to make sure transportation operations meet contractual and regulatory requirements • Maintain accurate compliance records and documentation • Identify potential compliance issues and proactively work with partners to resolve them • Travel throughout Florida and occasionally out of state to support service partners and district operations

Title: Associate Trade Compliance Manager Full time - Remote, São Paulo, Brazil - Remote, Lima, Peru - Remote, Colombia - Remote, Argentina - Remote, Mexico We have a vacancy for an Associate Trade Compliance Manager in our Global Clinical Supplies Team. The role can be fully home-based. A day in life: - Support developing Trade Compliance Import/Export strategy for studies. - Support ensuring studies are always in compliance with Trade Compliance, local regulations, company requirements and client needs. - Develop proficient communication and interaction with internal and external stakeholders to coordinate efforts, provide recommendations, and issue alerts to avoid obstacles during the import/export processes. - Develop Trade Compliance Import/Export strategy and serve as the primary point of contact and escalation for Trade Compliance and Import/Export matters for low complexity assigned studies. - Stay up to date with new processes and regulations concerning Trade Compliance and Import/Export. - Support process improvement initiatives. Keys to success: Education and Experience: - Bachelor's degree or equivalent and relevant formal academic/vocational qualification - Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). - Prior experience in clinical research, specifically in clinical supplies import/export, is preferred. In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: - Good understanding of import/export operations, local and global regulations and clinical trial supply operations - Good interpersonal, planning, organizational, problem-solving and decision-making skills - Good understanding of the Microsoft Office suite - Good focus on customers and attention to detail - Ability to work as team, as well as work independently with substantial mentorship - Fluency in English (reading, writing and speaking)