12 oct
|
Cytel
|
Cantabria
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/ADa M 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.
📌 Senior statistical programmer for clinical trials & sas (Cantabria)
🏢 Cytel
📍 Cantabria