Position Purpose: The Director, Senior Global Regulatory Lead (Sr. GRL) in Global Regulatory Strategy (GRS) is a member of the respective GRA GRS Therapeutic Area and contributes to the vision and goals of CSL as follows: Develops a global, integrated regulatory strategy ensuring innovative and scientifically sound regulatory approaches for assigned products, with a patient-centric focus and appropriate risk-taking to achieve successful regulatory outcomes from early development through post-marketing lifecycle activities. Acts as a key member and single GRA representative for Product Strategy Teams (PST) and related global R&D/commercial teams, while leading the Global Regulatory Affairs Strategy Team (GRAST) to ensure alignment and a unified regulatory voice. Leads health authority interactions (FDA, EMA) and builds productive relationships to drive positive regulatory outcomes globally. Engages GRAST members to deliver regulatory outputs, fosters accountability and collaboration, and serves as decision-maker/approver for regulatory deliverables. Ensures strong communication between regulatory and R&D teams. For selected roles, manages Regional Regulatory Leads and supports their development and career growth. Main Responsibilities and Accountabilities: Builds strong relationships with Product Strategy Teams, Clinical Development Teams, Safety Management Teams, and other stakeholders to ensure effective collaboration and communication. Manages strategic relationships with key health authorities (FDA, EMA) and coordinates with regional leads for non-home country interactions. Acts as the single GRA reviewer/approver for key deliverables and participates in regulatory due diligence and senior-level discussions. Leads preparation of key regulatory documents and mentors GRAST members. Utilizes regulatory intelligence, analytics, and cross-functional expertise to develop global regulatory strategies. Promotes consistency, collaboration, and knowledge sharing a