GlobalStudyManager

Are you ready to orchestrate global clinical studies that deliver life-changing medicines to people with rare and devastating diseases? Step into a role where your leadership turns complex study plans into real-world outcomes for patients, from protocol development through study close-out and archiving. As a key member of a global study team, you will unite internal experts and external partners across multiple geographies and phases (I–IV, including non-interventional, post-authorization safety studies, registries, and early access programs). Your decisions will drive timelines, cost, and quality—accelerating access while safeguarding scientific and operational excellence. You will translate strategy into action—leading vendor oversight, aligning country teams, and ensuring first-time-right delivery. How will you bring clarity, pace, and confidence to a global program where every month matters for patients and clinicians? **Accountabilities:** * Vendor Strategy and Oversight: Define scope, negotiate expectations, and manage performance of CROs and service providers to timeline, budget, and quality; maintain documented oversight throughout the study lifecycle. - End-to-End Study Delivery: Coordinate delivery from Clinical Study Protocol through set-up, maintenance, database locks, CSR development, and archiving, ensuring alignment with the Study Lead and governance standards. * Cross-Functional Integration: Partner with Data Management, Procurement, Regulatory, Patient Safety, Quality Assurance, and country teams to remove barriers and optimize study execution. * Meeting Leadership and Engagement: Plan and contribute to internal and external forums, including Investigators’ and Monitors’ meetings, to drive clarity and commitment on milestones. * Budget Stewardship: Support the Study Lead with budget oversight and invoice reconciliation for external providers to maintain financial accuracy and predictability. * Study Documentation and Planning: Develop and maintain g