Cytel is seeking a Principal Statistical Programmer to work embedded with one of our pharmaceutical clients, with Cytel backing the program.
You will lead SAS programming, develop SDTM/ADaM specs, oversee CRO deliverables, and support regulatory submissions. Strong independence, leadership, and knowledge of FDA/ICH regulations are required.
This sponsor-dedicated role offers exposure to multiple studies and collaboration with cross-functional teams in a fast-paced biostatistics environment.
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📌 Senior Statistical Programmer for Clinical Trials (Santiago de Compostela)
🏢 Cytel
📍 Santiago de Compostela
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