Statistical Programmer - SAS & R Experience

About

Description

As a Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. In this role, you will develop and validate SAS and R programs for data presentations and analyses, and provide programming support to your multidisciplinary global project team.

Responsibilities

• Review SAPs and TFL shells from a programming perspective
• Advise on the development of complex TFL shells from a programming perspective
• Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets
• Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs
• Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs
• Respond to QA and client audits and support qualification audits
• Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business
• Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs)

Qualifications

• Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc
• Programming experience in R is required
• Business fluency in English – both spoken and written – is a must

Application instructions:

• To apply click on the apply button