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The Global Program Clinical Head leads clinical programs in neuroscience, overseeing strategies and execution for regulatory approvals and market access, interacts with stakeholders, and ensures team development.

The Associate Director leads statistical programming for clinical trials, ensuring collaboration, resource allocation, and compliance while mentoring team members and developing documentation.

The Head of Scientific Learning & Capability leads the design and implementation of capabilities across International Medical Affairs, enhancing performance through learning strategies and programs while collaborating with cross-functional teams and managing external partnerships.

The Global Program Associate Director will manage global drug development projects, facilitating strategies, communication, and issue resolution while ensuring effective operation of the Global Program Teams.

The Senior Principal Statistical Programmer leads statistical programming for clinical studies, ensures compliance with standards, supervises programmers, and delivers high-quality datasets and outputs.

Provide strategic legal counsel and risk management for CLS Operations, support compliance, manage BD/M&A activities, oversee regulatory materials, drive innovation, and engage with various stakeholders.

The Pricing Director drives pricing strategies for pharmaceutical products, collaborating with stakeholders to optimize brand value and market access while ensuring compliance and governance in pricing decisions.

Lead Clinical Development operational strategy, oversee processes, systems and quality frameworks, drive process improvements, enable inspection readiness, manage cross-functional initiatives, and develop the Business Solutions team to support Phase 2/3 trials and regulatory compliance.

Lead statistical work and innovative trial designs in collaboration with clinical teams to enable quantitative decision making across projects.

The Functional Excellence Lead drives operational advancement in monitoring practices, ensuring alignment with RBQM principles, and optimizing trial efficiency through innovative techniques and stakeholder collaboration.