• Provide operational and administrative support to ensure compliance processes, documentation, and reporting requirements are properly tracked, organized, and executed across the organization • Assist with coordinating internal compliance processes, maintaining regulatory documentation, and supporting cross-functional teams in meeting contractual and regulatory obligations • Coordinate and track Non-Disclosure Agreements (NDAs) with employees, consultants, partners, and vendors • Support consultant and vendor intake processes, including onboarding documentation, due diligence coordination, and compliance approvals • Maintain organized contract files and compliance documentation, ensuring required records are properly stored and accessible • Assist in maintaining the company’s compliance calendar, including tracking deadlines for regulatory filings, certifications, training, and reporting obligations • Support FOCI compliance tracking, including maintaining required documentation and assisting with monitoring reporting obligations • Coordinate internal approvals and documentation related to compliance matters • Assist in preparing materials for internal audits, compliance reviews, and regulatory reporting • Maintain compliance trackers, logs, and reporting tools to ensure visibility into key compliance activities • Work with cross-functional teams to ensure documentation and processes align with company policies and applicable regulatory requirements • Maintain strict confidentiality of sensitive information • Assist in the development and improvement of compliance processes and documentation management practices. • Perform other duties as assigned

• Provide quality leadership and direction to sponsor R&D stakeholders on GCP-related activities/issues and act as GCP expert/consultant for R&D colleagues. • Act as a Clinical Compliance member of clinical study teams for relevant Therapeutic Areas. • Develop strong relationships with R&D personnel across functions and teams providing coaching and compliance guidance as needed. • Collaborate with stakeholders in conducting ongoing risk assessment of clinical trial activity to identify priority studies, compliance metrics for tracking, high-risk vendors, and key compliance activities (i.e., protocol review, vendor evaluations, inspection readiness). • Identify and escalate significant quality and compliance issues to the Head of Clinical Quality & Compliance and relevant leadership, including the assessment of serious breaches. • Participate as a member of Contract Research Organization (CRO)/Vendor governance teams for assigned Therapeutic Areas/Studies. • Establish a relationship with CRO Quality Team members for the ongoing review of quality and compliance issues. • Participate in vendor evaluations as a Subject Matter Expert (SME) as needed. • Support clinical teams/functions in drafting responses and CAPAs to internal and external audit findings. • Provide support and guidance for sponsor Quality Management System activities including self-reporting deviations, root cause analysis, and CAPA plan development and evaluation. • Identify and anticipate trends in quality issues and collaborate with functional management to ensure risk-managed solutions are implemented in a timely fashion. • Maintain a high level of expertise in international GCP regulations and internal Policies and Procedures that may impact drug development. • Provide support and guidance during and following internal audits and external regulatory inspections (as required). • Provide expertise and consultative guidance on business initiatives involving systems, processes, procedures, regulations, and tools intended for use in clinical trial conduct and/or regulated drug development activities. • Lead / manage inspection readiness activities and ensure project teams are trained and prepared for regulatory inspections.

• Review ad creatives (texts and visuals) to ensure compliance with the policies of advertising platforms (e.g., Facebook, TikTok, Google). • Conduct pre-moderation of client creatives, give actionable feedback, flag potential violations, and help mitigate risks of account bans. • Maintain records of policy violations and answer internal/external questions related to ad placement rules. • Participate in team syncs and collaborate with international colleagues (communication in English).

• 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.