Statistical Programmer, SAS

November 7

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Parexel

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Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+

💰 Venture Round on 1990-01

Description

• Support various SAS® programming activities related to clinical study data analysis and reporting • Produce analysis datasets, tables, figures, and data listings • Ensure first-time quality, traceability, and regulatory compliance • Improve/develop SAS® programming skills and broaden knowledge of clinical trial industry • Participate in preparation of electronic submission packages according to industry standards • Support response to regulatory agency questions • Prepare input to publications and conference materials • Develop statistical knowledge using 4GL and different SAS® procedures.

Requirements

• Knowledge and experience in SAS® software • Experience in 4GL language • Understanding the principles of statistics • Attention to detail with a focus on quality • MSc/PhD degree in statistics, econometrics, mathematics, informatics or a related field or equivalent professional experience • Experience in Clinical Research will be an asset.

Benefits

• private medical care at LUX MED • life assurance • pension scheme • Cafeteria system • lunch vouchers • more!