• Lead the Central Statistical Monitoring (CSM) team within the Global Statistics department • Provide statistical design, interpretation, and governance for monitoring activities • Develop, validate, and operationalize statistical monitoring indicators and models • Act as the CSM statistician interfacing with clinical study statisticians and other stakeholders • Collaborate with governance bodies to define statistical thresholds and signal characterization methods • Produce tiered deliverables for various stakeholders • Develop and deliver training modules for clinical monitors, safety officers, and study teams • Define KPIs for CSM effectiveness and monitor performance dashboards

• Lead an enterprise mindset across the Radioligand Therapies (RLT) regional ecosystem. • Develop, orchestrate, and execute the RLT priority ecosystem customer engagement strategy. • Build and maintain key business relationships with C and D suite personnel. • Understand the needs of the target ecosystem archetype customers at all levels. • Develop and drive strategic plans, collaborating with IFST members on pre-launch/launch strategy. • Identify opportunities for collaboration and engagement with ecosystem C-Suite, D-Suite, and other decision-makers. • Provide alternatives and solutions where challenges and ambiguity exist.

• Provides inspirational leadership and direction to a team of Clinical Account Managers (CAM) to successfully achieve performance objectives. • Achieves or exceeds goals through motivational leadership & strategic sales approach. • Creates a team culture which encourages continued growth and provides consistent recognition. • Challenges the CAM to continue self-development in their current role and for future opportunities. • Drives business by observing CAM interactions with key customers, peer collaboration, meeting participation & presentations, providing them with individual coaching, feedback to maximize effectiveness & impact with their customers. • Demonstrates understanding of the reimbursement and distribution model and works closely with Field Reimbursement Managers to ensure seamless delivery to customers. • Proactive talent scout for the organization with proven experience attracting, developing and retaining talent. • Utilizes a strategic approach to analyze their marketplace, uncover sales growth opportunities and capitalize on all competitive advantages. • Consistently challenges oneself to grow and develop further as a sales leader. Asks for feedback to raise awareness and gain insight into one's strengths and developmental needs. • Works collaboratively across functional areas by serving as a resource within one's region and by leveraging the expertise of others. • Actively seeks to discover and meet the needs of internal and external customers by building relationships and delivering innovative solutions. • Facilitates regular interactions and networking opportunities with key opinion leaders (KOLs) in the oncology field. • Fosters collaboration across different functional areas (e.g., sales, marketing, medical affairs) to ensure a cohesive approach to market challenges. • Utilizes data analytics to identify trends and opportunities in the oncology market. • Emphasizes Sobi’s commitment to improving the lives of patients with rare diseases in marketing and sales efforts. Develop effective business plans and sales strategies based on comprehensive market analysis.

• Define and implement QC strategy aligned with company objectives. • Partner with Analytical Development, Quality Assurance, CMC, and Regulatory Affairs teams to ensure cross-functional alignment in program planning and execution. • Serve as the primary QC liaison with CTOs/CMOs, driving accountability and timely delivery. • Communicate program status, risks, and mitigation strategies to senior leadership. • Collaborate with CMC Ops to align QC deliverables (specifications, stability data, method validations) with manufacturing and supply chain timelines. • Identify potential risks and implications raised from QC data, and drive technical risk mitigation in collaboration with internal and external teams. • Oversee outsourced QC testing activities, including raw materials, in-process, release, and stability testing. • Establish KPIs and governance processes to monitor vendor performance. • Ensure QC activities comply with cGMP, ICH, FDA, EMA, and other relevant guidelines. • Review and approve QC documentation, including test methods, protocols, and reports. • Establish, maintain, and update product specifications in alignment with regulatory expectations. • Design and oversee stability programs for clinical and commercial materials. • Provide oversight of outsourced complex investigations, including out-of-specification (OOS), out-of-trend (OOT), and atypical results, ensuring robust root cause analysis and CAPA implementation. • Ensure method validation, transfer, and lifecycle management are executed to regulatory standards and program timelines. • Collaborate with Analytical Development to provide technical guidance on analytical methods (e.g., potency assays, binding assays, HPLC, ELISA). • Support regulatory submissions through review and/or authorship of relevant dossier sections.