• Provide support on global trade compliance with a focus on export controls, product classification (ECCN), licensing, and permitting requirements • Analyze and interpret complex trade regulations and apply them to business operations across APAC • Support the regionalization of global trade compliance programs including restricted party screening, customer due diligence, and end-use/end-user reviews • Train, mentor, and support trade compliance personnel across APAC region

• Provide support on global trade compliance with a focus on export controls, product classification (ECCN), licensing, and permitting requirements • Analyze and interpret complex trade regulations and apply them to business operations across APAC • Support the regionalization of global trade compliance programs • Train, mentor, and support trade compliance personnel across Greater China and the broader APAC region

•Oversee and manage MLR review and approval submissions for Marketing, Medical Affairs, and Corporate Communications materials. •Partner with Medical Affairs teams to ensure appropriate submission ownership and coordination of review materials. •Coordinate MLR review meetings and ensure timely routing of materials to designated reviewers. •Maintain and manage the Master MLR Review Schedule across all business functions. •Develop, maintain, and communicate a weekly MLR 'Hot Sheet' highlighting all active and upcoming review activities requiring approval. •Track review status, approvals, reviewer comments, revision cycles, and final disposition of materials. •Collaborate with agencies, content creators, and internal library resources to ensure supporting references, journal articles, and documentation are appropriately maintained within Zotero and related content repositories. •Partner with leadership to identify workflow efficiencies and recommend process improvements to enhance review timelines and stakeholder experience. •Ensure proper version control and archival of approved materials and supporting documentation. •Maintain audit-ready records for all promotional review activities and approvals. •Manage tracking systems for FDA submissions, OPDP correspondence, advisory comments, approval records, version histories and compliance documentation •Generate and distribute MLR metrics, dashboards, and reporting to support business and compliance objectives. •Conduct training sessions for internal teams, external agencies, and business partners on promotional compliance requirements and MLR best practices.

• Litigates low to moderate complexity and exposure cases and performs duties necessary from intake to trial and/or settlement. • This includes but is not limited to preparation of pleadings, motions, discovery, and briefs. • Attends hearings, conferences, interviews, mediations, arbitrations, and/or trials. • Proactively informs leadership of case handling opportunities and challenges encountered. • Consults with the Claims Department on the legal aspects of files and jurisdictional issues. • Performs other tasks or duties to ensure efficient case management. • May handle second chair trials and handle trials in cases with moderate complexity and/or exposure. • Provides support to senior attorneys in cases of greater complexity and/or exposure and receives developmental assignments of matters that are of high complexity and/or exposure.