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.

The role oversees Clinical Development compliance with regulations, leads clinical trial readiness, and manages corrective actions. It involves training compliance and continuous assessment of quality risks.

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

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.

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 Senior Principal Statistical Programmer leads statistical programming for clinical studies, ensuring quality deliverables, compliance with industry standards, and managing programming teams. Responsibilities include coordinating activities, developing statistical solutions, and maintaining relationships with cross-functional teams.

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

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.

Serve as strategic global legal partner for the Immunology Therapeutic Area, providing counsel on compliance, contracts, BD/M&A, regulatory/promotional reviews, alliance management, training, and governance. Lead legal strategy for assigned assets, coordinate with regional and country legal teams, and drive initiatives to strengthen capabilities and mitigate legal and business risks across development and commercial activities.

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

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 Global Monitoring Functional Excellence Director leads field monitoring strategies at Novartis, enhancing operational efficiency and ensuring compliance with regulations through innovation and process improvements.

Lead development of high‑quality, compliant scientific and medical materials (slide decks, congress content, advisory board materials). Synthesize complex clinical data, ensure scientific accuracy and governance, manage multiple projects across brands, and collaborate with cross‑functional stakeholders in a matrixed international environment.

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

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

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.

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

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

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.