Description
Statistical Programmer - Amsterdam - 12 Month Contract
Main Responsibilities:
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Provide input as appropriate to all meetings, discussions and activities covering all SAS programming aspects for assigned clinical trials.
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Programming of analysis datasets, pooled datasets, listings, summaries, figures and tables for the reporting and analysis of the clinical trials and of the ISS and ISE according to the specifications
Key Skills and Qualifications:
- Excellent SAS programming skills with 5 years experience in the pharmaceutical industry
- Proven SAS programming experience in the area of analysing & reporting of clinical data
- Profound knowledge in Statistics, degree in Statistics is a plus
- Knowledge in CDISC standards, especially SDTM, ADaM, Terminology is a plus
If interested please respond with an updated C.V.