The Global Program Clinical Head leads clinical programs in neuroscience, overseeing strategies and execution for regulatory approvals and market access, interacts with stakeholders, and ensures team development.

The Clinical Biospecimen Senior Scientist manages biospecimen operations for clinical trials, ensuring compliance with processes and protocols, oversees sample management, and collaborates with stakeholders for clinical sample assessments and logistics.

The Head of AI Transformation & Enablement leads AI integration into Global Clinical Operations, overseeing AI initiatives and workforce enablement while driving cross-functional collaboration and compliance with industry regulations.

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 GCP Compliance Manager oversees compliance for clinical trials, provides support to Clinical Trial Teams, and coordinates audits and inspections, ensuring adherence to GCP standards.

The Senior Global Process Owner leads the design and management of risk-based quality management processes in clinical trials, ensuring compliance and continuous improvement.

The Senior Global Process Owner leads the end-to-end clinical trial process, ensuring compliance, governance, and continuous improvement through collaboration and process optimization.

The Associate Manager in PE Governance Office oversees operational support, ensuring compliance in contract management and funding activities for patient engagement projects. The role involves collaboration with legal teams, process optimization, and effective stakeholder communication.

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.

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 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.

Lead the submission production capability and strategy for regulatory affairs, ensuring alignment with organizational goals and overseeing digital technology adoption.

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

The Study Start-Up Senior Lead is responsible for leading global SSU activities, managing teams, and ensuring timely trial document preparation for submissions and site activations.

The Study Start-Up Lead manages global SSU activities, overseeing document readiness, risk management, and vendor activation to ensure timely trial execution.

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

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

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

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