Manager Risk ManagementREQ-10084431Jul 28, 2026SpainAvailable in: English### SummaryReady to make a direct impact on patient safety across the globe? At Novartis, every decision we make is driven by our purpose to reimagine medicine for patients.

As Manager Risk

Management, you will be at the heart of that mission, helping to shape and maintain the safety strategies that support life-changing medicines throughout their lifecycle. In this highly visible global role, you will collaborate with medical safety leaders, cross-functional experts, and international stakeholders to drive regulatory excellence, influence risk management activities, and ensure the delivery of high-quality safety documentation that protects patients and builds trust with health authorities worldwide. Hybrid (12 days per month onsite) Relocation Support: Novartis is unable to offer relocation support - please only apply if this location is accessible to you.### About the RoleKey Responsibilities Partner with Global Product Safety Leaders and cross-functional teams to drive effective risk management strategies.

Lead the coordination and delivery of high-quality, regulatory-compliant Risk Management Plans and Aggregate Reports.

Coordinate contributors across functions to secure quality content, annexes, and supporting documentation.

Review risk management documents for consistency, accuracy, and compliance with regulatory requirements.

Ensure timely development, review, and submission of safety documentation to general health authorities.

Manage Health Authority commitments and track implementation activities across global and local stakeholders.

Support responses to Health Authority feedback and ensure approved requirements are effectively implemented.

Provide training, guidance,



and subject matter expertise on risk management processes and requirements.

Contribute to process improvement initiatives, digital innovation, and Artificial Intelligence-enabled solutions.

Represent Risk Management expertise in inspections, audits, and cross-functional quality improvement projects.Essential Requirements Minimum 5 years of experience within the pharmaceutical industry, preferably in drug safety, clinical research, or regulatory affairs and Minimum 1 years of Global RMP management experience within the pharmaceutical industry.

Bachelor's degree in Life Sciences, Pharmacy, Medicine, or a related scientific field.

Fluent written and spoken English with strong scientific communication and document writing skills.

Strong knowledge of global regulatory requirements, clinical drug development, and pharmacovigilance processes.

- Ability to analyze and interpret safety and efficacy data and translate findings into clear regulatory documentation.**In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. Read our brochure to learn more about our global total rewards offering: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. Collaborating, supporting and inspiring each other. Research & DevelopmentFull timeRegularNoResearch & DevelopmentDevelopmentSpainREQ-10084431### Manager Risk ManagementApply to Job

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