DMCP-0, Senior Specialist, Clinical Data programming

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.