Medical Director Safety

Clinical Research Unit - Nestlé Research

Welcome to Nestlé Research, a global organization, with most of our passionate team located in Lausanne, Switzerland! Our work is powered by five specialized Nestlé Institutes and key strategic functions. Here, we embrace fresh thinking and collaborate to create amazing solutions. How about taking a step inside our organization and discover the exciting research activities and expertise that drive us forward? Want to learn more!

At Nestlé Research, we place people**atthecoreof everything we do, driven by a passion for innovation that inspires us to embrace change. Our commitment to staying at the forefront of science allows us to make a meaningful**impact on our world, fostering a culture of creativity and**growth. Join us in our mission to**inspire peopleand ignite**innovation**as we work together to shape a better future.

Position Snapshot: Your opportunity to #breakthrough with us!

Location: Clinical Research Unit, Nestlé Research, Lausanne, Switzerland Company: Société des Produits Nestlé S.A.

Act. Rate: Full-Time Actual Rate 100% Type of contract: Permanent

What we offer at Nestlé

Exciting opportunities to develop your career your way

Flexible working arrangements - facilitating creativity and collaboration. A culture of respect, with diversity, equity and inclusion at its core.

A dynamic international environment empowering you to learn, develop and grow. Don-t hesitate to connect with us during the recruitment process to learn more

Position Summary

As a Medical**DirectorforClinicalTrial/ResearchSafety**you will provide expert safety leadership and input to clinical development programs for nutritional solutions and therapeutics across the lifespan, and ensure safety compliance with regulatory frameworks applicable to pharma, medical nutrition and food for medical purposes (FSMP).

A Day in the Life of a Medical Director Safety

• Responsible for building safety assessments and safety management plans optimized for trial design, conduct signal detection, monitoring, evaluation, interpretation and appropriate management & reporting of safety information such as annual safety reports, based on data from all relevant sources
• Lead safety input to Data Safety Monitoring Boards charters, aggregate safety reports (DSUR/ASR where applicable), and risk management plans; contribute to Safety & Risk Management Team (SRMT) and signal review forums
• Coordinate the management of internal trial safety boards and committees
• Drive safety strategies and ensure safety compliance with applicable regulatory frameworks, in close collaboration with clinical development, data management, medical, scientific and regulatory affairs teams as well as trusted external providers for case processing
• Engage with key opinion leaders (KOLs) and investigators, to shape safety strategies, including those informed by independent safety data monitoring committees, and to optimize alignment with clinical trial designs
• Respond to inquiries regarding safety issues and collaborate closely with regulatory teams for health authority responses for nutritional solutions
• Support a core team working on end-to-end pharmacovigilance for nutrition therapeutics with signal evaluation and risk management
• This position will have functional/ dotted line alignment to internal patient safety & risk management governance frameworks

What Will Make You Successful

• Medical degree, MD/PhD, preferably with specialization in one of the following areas: internal medicine / gastroenterology / pediatrics / clinical pharmacology. Swiss medical practice license is a plus
• At least 5 years- experience in clinical research and safety, in development or operations (pharma, biotech, diagnostics, medtech, nutrition, or CRO settings)
• Experience and proven impact in leading safety management in complex clinical trials, including issue management and regulatory frameworks of nutrition and medical nutrition
• Expertise in preparation of clinical safety assessments and regulatory submissions involving safety information
• Strong strategic acumen with experience in collaborating across matrixed, cross-functional teams
• Ability to analyze, interpret, and communicate complex clinical and scientific information
• Effective external engagement capabilities (KOLs, agencies, investigators, safety vendors)
• Ability to balance urgency, quality, and compliance in dynamic development environments

Nestlé is committed to the accessibility of its recruitment process. If you require an adaptation during the recruitment process, please do let us know so we can support you effectively. All information will be treated confidentially.

At Nestlé, we want to help shape a better and healthier world, inspire people to live healthier lives and deliver impact at a scale and pace that makes a difference. We do this by fostering a diverse, friendly, supportive, and collaborative environment, that creates positive disruption, embraces innovation, and empowers people and teams to win. We aim to hire friendly, respectful, inspiring people who care about the people-s lives that we touch every single day.

Be a force for good. Join Nestlé and visit us on www.nestle.com.

Lausanne, CH