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

Accountable for GCP compliance oversight in Global Clinical Operations, managing audits, inspections, quality issue resolution, and promoting compliance culture.

The Solution Design Associate Director will translate business challenges into innovative solutions, lead technical teams, and enhance business operations through strategic design and project management.

Lead quality oversight for clinical trials, ensuring compliance with health regulations and internal standards while managing quality risk and incident management processes.

The Clinical Quality Assurance Program Lead provides oversight for clinical trials ensuring compliance with regulations, quality strategy implementation, and risk management while leading QA initiatives and collaborating with global teams.

Oversee authoring, formatting, and publishing of Clinical Study Report (CSR) appendices, ensuring compliance with regulatory standards and improving submission processes. Manage vendor oversight and collaborate with cross-functional teams to enhance document readiness and quality.

The Clinical Development Director leads clinical activities, ensuring successful trial execution, and collaborates with stakeholders while mentoring team members.

The Vendor Program Strategy Director oversees vendor activities for clinical studies, ensuring compliance with regulations, managing supplier performance, and defining program strategies in collaboration with various stakeholders.

The Vendor Performance Analysis Manager analyzes business processes to optimize costs, improve supplier performance, and supports sourcing strategies. Responsibilities include data analysis, financial modeling, and collaboration with cross-functional teams to enhance operational efficiency and vendor relationships.

The Senior Principal Biostatistician leads statistical work for clinical trials, implements innovative designs, and provides statistical expertise for drug development.

The Associate Director will lead genetic toxicology studies, provide expert assessments, ensure regulatory compliance, and collaborate with teams on drug development.

The Associate Director, Statistical Programming leads statistical programming for clinical trials, ensuring collaboration, quality, and compliance while mentoring teams and overseeing resource allocation.

Develop and maintain R packages for clinical trial data workflows, build Shiny applications, and promote data science best practices within the organization.

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

The Associate Director, Business Operations leads GMA functional strategy, manages transformation projects, and integrates innovative solutions for operational effectiveness.

The role manages and enhances project and pipeline data, develops actionable reports for decision-making, and ensures data accuracy and accessibility. It requires collaboration with teams to optimize performance and ensure compliance with governance standards.

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.

Lead cross-functional teams to develop and submit evidence dossiers for HTA processes, ensuring high-quality submissions and engagement with HTA bodies.

As Director, you'll lead strategic planning and execution of clinical programs, manage resources, ensure compliance, and drive team performance across global trials.