Statistical Programmer I, SAS experience

November 9

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Parexel

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 SAS® programming activities related to clinical study data analysis • Produce analysis datasets, tables, figures, and data listings • Ensure first-time quality, traceability and regulatory compliance • Prepare electronic submission packages and response to regulatory agency questions • Develop statistical knowledge using 4GL and 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

• Competitive financial packages • Training and development • Healthy work/life balance

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