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

Lead end-to-end clinical development for cardio-metabolic programs, providing scientific and clinical oversight, regulatory input, safety leadership, cross-functional collaboration, and training. Drive execution of clinical plans, data review, and stakeholder interactions to support registration and program decisions.

The Lead Central Monitor drives clinical trial monitoring excellence at Novartis, managing a team to ensure data integrity and effective risk management. Responsibilities include strategy development, risk oversight, team leadership, and oversight of monitoring processes and technologies to ensure quality in clinical data.

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

Lead cross-functional global clinical trial teams to plan, execute, and deliver medium-to-complex clinical studies. Manage timelines, budgets, risk, vendor and stakeholder relationships, drive operational excellence, ensure compliance with GCP/ICH and regulatory requirements, and support study close-out and reporting.

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

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

The Risk Surveillance Lead ensures RBQM practices, oversees quality risk governance in clinical trials, and collaborates cross-functionally to enhance trial quality.