My client a leading pharmaceutical company currently has 2 new opportunities for a Principal SAS Programmer and a Senior SAS Programmer to join their growing departments. You would be based in there head office in Switzerland.
PURPOSE OF ROLE
- Independently, function as a lead statistical programmer coordinating programming aspects for a clinical trial.
- For clinical trials requiring routine or complex data manipulation and analysis, independently program (or write validation programs for) and document tables/listings/figures/analysis datasets.
- For integrated safety and efficacy summaries for regulatory submissions, independently program (or write validation programs for) and document tables/listings/figures/analysis datasets.
- With direction, provide input into general standardization efforts and create (or validate) global macros that streamline repetitive operations
- May administratively and functionally manage up to two statistical programmers with respect to statistical programming strategy, deliverables, processes, and professional development.
Qualifications
- Ideally a BSc or MS (in a numerate discipline, preferably in Statistics, Computer Science, or Mathematics)
- Fluent in English (French or German is a plus)
- Strong industry experience in the Pharmaceutical/Biotechnology industry in clinical development
- Expertise SAS/BASE, SAS/STAT
- Knowledge of SAS/CONNECT, SAS/MACRO, SAS/GRAPH, SQL
- Knowledge of relevant regulatory guidelines applicable to clinical development
- Familiarization with or ability to develop an understanding of relevant therapeutic areas
This job was posted 30+ days ago, and has expired.
