Jobs at Novartis

Provide strategic legal counsel in the pharmaceutical sector, manage legal risks, negotiate agreements, lead litigation, and develop team policies.

The SSO Study Start-Up Manager oversees study planning, SSU activities, and ensures compliance with regulations and timelines for clinical trial projects.

The Expert Scientific Writer leads the development of scientific publications, translating complex clinical data into clear content, and ensuring accuracy while collaborating with cross-functional teams.

The ESG FRA Process & Project Expert coordinates ESG reporting projects, supports governance, ensures compliance with regulations, and enhances non-financial reporting processes.

The Imaging Operations Manager oversees imaging strategy implementation in clinical studies, coordinates vendor interactions, ensures adherence to protocols, and manages service quality and risk assessment.

This role involves leading safety input and strategy in clinical development, managing safety issues, overseeing signal detection, and collaborating on regulatory inquiries, while contributing to departmental goals in a director-level capacity.

The Global Program Safety Lead will oversee safety input for clinical development, prepare safety strategies, manage safety issues, and lead cross-functional teams in drug development.

The Director of Portfolio Scientific Communications at Novartis will lead global scientific communication strategies in Immunology, focusing on narrative development, publications, and medical education to enhance HCP understanding and improve patient care.

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

The Senior Administrative Assistant provides comprehensive support to leaders, managing calendars, travel arrangements, document preparation, and compliance activities.

The Executive Director leads the Pricing & Contracting team, develops pricing strategies, collaborates across functions, and advises on pricing-related topics while mentoring staff.

The Senior Principal Statistical Programmer leads statistical programming for clinical studies, ensures compliance with standards, supervises programmers, and delivers high-quality datasets and outputs.

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.

Lead planning, execution, and reporting of global medical studies in Neuroscience, ensuring quality, compliance, and timely delivery. Collaborate with stakeholders and manage operational risks.

Lead Clinical Development operational strategy, oversee processes, systems and quality frameworks, drive process improvements, enable inspection readiness, manage cross-functional initiatives, and develop the Business Solutions team to support Phase 2/3 trials and regulatory compliance.

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

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 the legal strategy for Value & Access in international markets, advising on pricing, reimbursement, HTA, and public procurement while managing regulatory and access risks.

The Global Regulatory Affairs Associate Director leads regulatory strategies, manages submissions, and collaborates with teams to ensure compliance and facilitate approvals throughout the product lifecycle.

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