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Lead statistical programming activities for clinical studies, ensuring compliance with standards and providing high-quality deliverables. Collaborate with teams and mentor programmers.

The Study Start-Up Senior Lead is responsible for leading global SSU activities, managing teams, and ensuring timely trial document preparation for submissions and site activations.

The Central Monitor oversees clinical trials via data surveillance and centralized monitoring, ensuring data quality and regulatory compliance.

The Lead Central Monitor oversees clinical trial monitoring by managing a team, developing strategies, ensuring data integrity, and fostering collaboration. They drive risk management and process improvements while supporting clinical trial teams in their execution.

Provide strategic legal counsel in the pharmaceutical sector, manage legal risks, negotiate agreements, lead litigation, and develop team policies.

The ESG FRA Process & Project Expert coordinates ESG reporting projects, supports governance, ensures compliance with regulations, and enhances non-financial reporting processes.

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.