The Site HSE Head & Cluster Lead is responsible for executing HSE programs at the Novartis Corporate Centre while ensuring compliance with global initiatives and local requirements. This role involves direct management of HSE service providers and collaboration with various departments to implement HSE strategies, handle incidents, and ensure stakeholder engagement.

The CSR Appendices Oversight Manager is responsible for managing and overseeing the authoring, formatting, and publishing of CSR appendices for regulatory submissions to health authorities. The role involves collaboration with cross-functional teams, ensuring compliance with guidelines, and driving process improvements in clinical document management.

The Sales & Marketing Lead will oversee the sales and marketing functions in the Neuroscience team, focusing on achieving sales, market share, and profitability targets. The role involves strategic marketing development, financial performance oversight, and ensuring compliance with ethics and risk policies.

The Senior Global Process Owner is accountable for the design, management, and compliance of end-to-end business processes in clinical development. Key responsibilities include process governance, risk management, performance monitoring via KPIs, leading process improvement initiatives, ensuring regulatory compliance, and collaborating across functions to enhance operational efficiency.

The Senior Principal Biostatistician is responsible for statistical activities in clinical development, providing expert support in designing trials and reporting analysis. They drive innovative trial designs, guide teams, and ensure compliance with standards, while mentoring others and managing vendor relationships. This role requires advanced statistical knowledge and strong communication skills.

The GCP Compliance Manager oversees compliance in GCO activities, focusing on quality and risk management. Responsibilities include managing audits, inspections, and systemic quality issues, promoting a culture of compliance, and collaborating with cross-functional teams to ensure adherence to GCP standards.

The GCP Compliance Manager oversees compliance in clinical operations and trial management, working with teams to support quality assurance, manage audits and inspections, and promote a culture of compliance and ethics within the organization.

The GCP Compliance Manager (EMEA Hub) oversees compliance and control of regulated GCO activities, ensures effective quality oversight, manages issue handling during clinical trials, and liaises with domestic teams to promote a culture of compliance and adherence to standards within the organization.

The RWE Associate Director develops and executes strategies for Real World Evidence across molecules, focusing on non-interventional studies. They lead projects, ensure rigorous study designs, drive innovations, and effectively communicate findings to stakeholders. The role requires a strong background in Data Analysis, Epidemiology, and project leadership.

The Associate Director will lead analytics and insights generation to support key people and organizational projects, driving thought leadership, process improvements, and insights translation into actionable recommendations. Collaboration with various teams and stakeholders is essential, alongside the development of new service offerings and methodologies in analytics.

The Associate Director of Data Science will lead data-driven insights to enhance employee engagement, optimize talent acquisition, and refine workforce planning. Responsibilities include developing predictive models, utilizing machine learning algorithms, conducting statistical evaluations, collaborating on strategy design, and creating data visualizations. The role also involves exploring new data sources, ensuring compliance, and mentoring junior team members.

The Study Start-Up Senior Lead is responsible for leading global study start-up activities, ensuring timely document completion and submission for clinical trials. They manage a diverse team, oversee vendor activation, and maintain compliance with regulatory standards while driving performance and efficiency in clinical study start-up processes.

The Insights and Analytics Manager will analyze complex data sets to derive actionable insights, support marketing initiatives with data-driven recommendations, manage multiple analytics projects, and facilitate cross-functional collaboration. The role requires strong analytical skills and proficiency in CRM and data visualization tools.

The Commercial Excellence Lead drives initiatives to enhance customer engagement and optimize commercial strategies. Responsibilities include developing customer-centric strategies, leading omnichannel engagement, managing performance KPIs, and implementing business-critical systems in the pharmaceutical sector.

The Associate Director role focuses on providing reporting and analytics support across the People & Organization function. Responsibilities include defining KPIs, analyzing data to generate insights, maintaining reporting products on Power BI, and collaborating with teams to enhance data management and efficiency.

The Risk Surveillance Lead will drive the adoption of Risk-based Quality Management practices at the trial level, oversee implementation and continuous improvement efforts, and ensure effective risk management strategies are in place across clinical trials. They will facilitate risk assessments, maintain risk management documentation, and lead cross-functional teams to enhance clinical trial quality and compliance with regulatory standards.

The Study Start-Up Lead is responsible for planning and executing global start-up activities, ensuring timely completion of trial documents and tasks to enable submissions to health authorities and site activation. This role leads a team, collaborates with various stakeholders, and drives timelines and quality in clinical trial start-up processes.

The Associate Director, Data Engineering Lead will establish robust data assets to support clinical studies, guiding the execution of data engineering projects, developing data pipelines, and fostering collaboration across teams. Key responsibilities include managing project execution, ensuring compliance with standards, promoting innovative practices, and maintaining high-quality outcomes.

The P&O Technology Product Expert supports the management and maintenance of P&O technologies, resolving issues and enhancing user experiences. Responsibilities include change and release management, technical support, vendor management, compliance, and communication with stakeholders about system performance and improvements.

The P&O Technology Product Owner manages and maintains various P&O technologies, ensuring optimal configuration, providing technical support, and fulfilling technology service requests. The role collaborates with vendors, monitors data quality, and produces reports to enhance user experience and compliance with regulatory requirements.