DMCP-0, Senior Specialist, Clinical Data programming

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:

Clinical data is the backbone of every decision made in drug development — and in this role, you are at the center of it. As a Senior Specialist in Clinical Data Programming, you will design, develop, and own high-quality programming solutions that ensure the integrity, accuracy, and traceability of clinical trial data across the full study lifecycle. Working independently within a globally connected team, you will deliver validated programs for data quality surveillance, risk signal identification, and operational reporting, while contributing to the continuous improvement of standards, tools, and processes that power clinical development at scale.

Who You Are

• You hold a degree in Life Sciences, Computer Science, Mathematics, or a related field — or bring equivalent industry experience in clinical data programming.


• You have 7 or more years of hands-on experience as a clinical data or clinical monitoring programmer in the pharmaceutical or biotechnology industry.


• You bring comprehensive knowledge of SAS (Base and Macro) and  Qlik and R, alongside proficiency in SQL and at least one additional language such as Python; experience with EDC systems (e.g., Medidata Rave, InForm) and CDISC standards including SDTM and define.xml is essential.


• You develop, validate, and maintain programs for data quality checks, risk signal detection (KRIs/KQIs), and operational reporting — applying rigorous documentation discipline and GxP compliance awareness throughout.

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!