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Statistical Programmer

1 month ago

London, Greater London, 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 be responsible for developing, testing, and executing SAS programs to produce and validate CDISC SDTM and ADaM datasets, tables, figures, and listings.

Key Responsibilities

  • Develop and review specification for SDTM datasets and ADaM datasets for safety data, TFL shells, and other specifications.
  • Develop and review electronic data submission package (SDTM annotated CRF, define.xml, Study/Analysis Data Reviewer's Guide) for high complexity studies.
  • Perform review and provide guidance on the development of the clinical database specification, data transfer agreement/specification, specification of tables, figures, and listings (TFL) shells.

Requirements

  • 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.
  • Hands-on expert level project statistical programmer experienced in providing programming leadership to projects.

About Us

At Worldwide Clinical Trials, we are a global, midsize CRO that pushes boundaries, innovates, and invents. We are a global team of almost 3,000 experts, bright thinkers, dreamers, and doers, and together, we are changing the way the world experiences CROs. Our mission is to work with passion and purpose every day to improve lives, and we are looking for others who value this same pursuit.