Statistical Programmer

4 weeks ago


Newcastle upon Tyne, Newcastle upon Tyne, United Kingdom Worldwide Clinical Trials Full time
About the Role

We are seeking a highly skilled Statistical Programmer to join our team at Worldwide Clinical Trials. As a Statistical Programmer, you will play a critical role in ensuring the accuracy and quality of our clinical trial data.

Key Responsibilities
  • Develop, test, and execute SAS programs to produce and validate CDISC SDTM and ADaM datasets, tables, figures, and listings.
  • Perform review and provide guidance on the development of the clinical database specification, data transfer agreement/specification, specification of tables, figures, and listings shells.
  • Develop and review specification for SDTM datasets and ADaM datasets for safety data, TFL shells, and other specifications, e.g., patient profiles, OPS reports.
  • Develop and review electronic data submission package (SDTM annotated CRF, define.xml, Study/Analysis Data Reviewer's Guide) for high complexity studies.
Requirements
  • Educated to degree level or equivalent.
  • Advanced SAS programming skills with expert knowledge in SAS/Macro, Proc Report, and ODS. Good working knowledge in SAS/Graph, Proc SQL, and SAS/STAT.
Why Join Us

At Worldwide Clinical Trials, we are committed to advancing science and improving lives. We offer a values-driven culture that empowers our team members to treat every clinical trial like a patient's life depends on it. Our leaders are in the trenches with you, committed to moving mountains for our customers.



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