Associate Analyst - Clinical Trial Supply

Work Your Magic with us!  

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your Role:

Successful candidate to join our Global CTS (Clinical Trial Supply) team in delivering exceptional support and services, including Finance, Contracts, eTMF Operations, Database Management, and KPI Management and also will be responsible for managing the day-to-day operations of the Global CTS team, ensuring high-quality support, and driving process improvements.

Who You Are:

Minimum Requirements:

• Postgraduate degree in Life Sciences, Biotechnology, or MPharm.
• Experience: 2 to 7 years.

Preferred Requirements:

• Support the coordination and management of clinical supply projects, including planning, scheduling, budgeting, and resource allocation.
• Archive clinical supply documentation in internal and external GMP and GCP systems.
• Organize and control the compilation of documents for approval by the competent person.
• Check the content and completeness of technical specifications, documents, and contract annexes, and archive them appropriately.
• Manage project documentation, including project plans, status reports, and meeting minutes.
• Create and review supply contracts and control budget/invoice approvals within the defined framework.
• Support post-trial reviews and identify opportunities for process improvement.
• Assist the Clinical Supply Manager and Coordinator with other project-related tasks as required.
• Ensure full GMP compliance and documentation for clinical supply activities, including returns, destruction, and full global traceability of Investigational Medicinal Products.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!