Clinical Study Report Developer

3 days ago


Gothenburg, Västra Götaland, Sweden TN Sweden Full time

Job Description

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As a Senior Statistical Programmer at TN Sweden, you will play a critical role in the development of clinical study reports. Your expertise in the SAS programming language will enable you to design and implement data management systems, perform statistical analyses, and create high-quality reports that meet regulatory requirements.

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Responsibilities:

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  • Design and implement data management systems using SDTM and ADaM datasets.
  • Perform statistical analyses and create statistical analysis tables, listings, and figures.
  • Validate datasets and all statistical outputs per prescribed gate checks.
  • Develop programming specifications and write programming code following established Good Programming Practices.
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Requirements:

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  • Master's or Bachelor's degree in Biostatistics, Statistics, Mathematics, or Computer Science.
  • 5+ years of experience in a Statistical Programmer role from CRO/Pharma with ADaM/SDTM/TLFs.
  • Excellent accuracy, attention to detail, problem-solving, organizational, and interpersonal communication skills.


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