Senior Analyst - Clinical Trial Coordinator

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:

As a Clinical Trial Coordinator within the Local-Regional Studies Support Office, you will play a meaningful role in keeping global clinical trials on track — ensuring the operational backbone of each study runs with precision, compliance, and care. Working as part of dedicated trial teams across a broad portfolio of local and regional studies, you will coordinate and support a range of essential trial activities, from budget and invoice tracking to quality issue support and regulatory reporting oversight. Clear guidance from senior colleagues will support your growth as you contribute directly to the quality and integrity of clinical development operations.

Who You Are:

• A bachelor’s degree or equivalent in a scientific field, with 1 to 2 years of experience in a clinical research-related role; candidates without a degree are welcome with a minimum of three years of relevant professional experience and additional qualifications demonstrating exposure to clinical research fundamentals.

• A foundational understanding of clinical operations and ICH-GCP guidelines, paired with comfort navigating the administrative and coordination demands of a clinical trial environment.

• Proficiency in standard office productivity tools — including spreadsheet, word processing, and presentation software — and some familiarity with clinical trial management systems.