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

In this role, you will manage administrative tasks, coordinate project activities, support the hiring process, and ensure effective communication within Global Medical Affairs.

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.

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

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 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.

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.

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

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.

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

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

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.