The AI Change Lead will drive AI adoption, enhance AI fluency, design training programs, and support leaders through organizational change initiatives.

Lead high-impact programs in consulting and program management, collaborating with cross-functional teams to enhance commercial and medical excellence using AI-driven solutions.

The Expert Scientific Writer is responsible for creating high-quality scientific content, mentoring team members, ensuring accuracy, and adhering to industry protocols during project execution.

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.

Responsible for creating complex scientific content and managing multiple projects across brands. Involves document preparation, compliance, training, and process improvement in clinical research.

Responsible for managing data management aspects of clinical studies, ensuring quality deliverables and compliance with industry standards, while leading functional activities and collaborating effectively with teams.

Lead the Marketing Cloud Intelligence team, designing data solutions, managing stakeholder engagement, and optimizing reporting capabilities to support business goals.

Lead the development and execution of HEOR strategies to demonstrate product value and support commercialization through research and collaboration with global teams.

The role involves developing AI algorithms for drug discovery, collaborating with researchers, and driving AI innovations in biomedical research.

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

Manage TMF documentation for M&A projects, oversee transitions, develop processes, and ensure compliance in clinical document management.

The Principal Clinical Data Scientist manages Data Management for clinical studies, ensuring compliance with good practices, leading quality deliverables, and implementing training strategies.

The Principal Clinical Data Scientist manages data management for studies, leads quality deliverables, ensures compliance with GCP, and develops training strategies. They also coordinate data managers, handle risk management strategies, and participate in audits and inspections.

The AI Search & SEO Manager will develop and implement AI search strategies, manage research and optimization efforts, and lead tool partnerships to enhance AI visibility for Novartis brand websites.

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.

The role involves leading clinical data management tasks, ensuring quality and compliance in data for clinical trials, collaborating with teams, and supporting junior staff.

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

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.

Leading the Data42 team, you will manage data engineering and product development, ensuring quality and accessibility of data solutions across Novartis.