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The Associate Director oversees congress operations, ensuring alignment with strategic objectives, managing cross-functional teams, and maintaining high stakeholder relations while driving innovation and compliance.

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

The Director - Genetic Toxicology Expert will oversee genetic toxicology studies, provide expert insights for drug development, and ensure regulatory compliance while leading cross-functional teams.

Lead the implementation of innovative trial designs and statistical methods in drug development while contributing to strategic decision-making across cross-functional teams.

Lead data and analytics strategy for Value and Access; strengthen governance, manage budgets, and enable data-driven decision-making across healthcare operations.

The Associate Director of Clinical QA will oversee quality compliance for clinical trials, manage risks, and lead quality initiatives to ensure patient safety and adherence to regulations.

The Senior Scientific Engagement Manager is responsible for leading scientific events, project planning, and ensuring impactful delivery while utilizing digital technologies for efficiency.

The Clinical Development Director leads clinical programs, ensuring delivery of clinical goals, collaborating across teams, managing trial data, and contributing to regulatory documents amidst a focus on patient safety.

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.

The Regional Head CRMA EU oversees clinical research programs, driving innovation and quality in drug development. They lead a large team, manage complex projects, and establish relationships to ensure successful trial execution.