Senior Statistical Programmer

7 days ago


London, Greater London, United Kingdom Worldwide Clinical Trials Full time
About the Role

We are seeking a highly skilled Senior Statistical Programmer to join our team at Worldwide Clinical Trials. As a key member of our data science team, you will be responsible for developing and implementing statistical programming solutions to support our clinical trials.

Key Responsibilities
  • Develop, test, and execute SAS programs to produce and validate CDISC SDTM and ADaM datasets, tables, figures, and listings (TFL).
  • 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.
  • 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, Study/Analysis Data Reviewer's Guide) for high complexity studies.
Requirements
  • Must be computer literate and numerate with a willingness to adapt to various computer systems.
  • Hands-on expert-level project statistical programmer experienced in providing programming leadership to projects.
  • Statistical programming skills and knowledge across a broad range of applications together with key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change.
What We Offer

As a Senior Statistical Programmer at Worldwide Clinical Trials, you will have the opportunity to work on complex clinical trials, develop your skills in statistical programming, and contribute to the success of our data science team. We offer a dynamic and collaborative work environment, opportunities for professional growth and development, and a competitive compensation package.



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