- Generate tables, listings, and figures (TLFs) for clinical study reports and regulatory submissions.
- Contribute to the development and review of Statistical Analysis Plans (SAPs).
- Evaluate the quality, accuracy, and consistency of all statistical programming deliverables.
- A strong foundation in statistics.
- Solid understanding of clinical trial data structures.
Senior SAS Programmer - Italia - Warman O'Brien
Descrizione
Senior SAS Programmer
An experienced statistical programmer is sought to join a collaborative and high-performing team in North Italy.
Key Responsibilities:
The ideal candidate has:
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