Senior Biostatistics Programmer Lead

1 week ago


Dublin, Dublin City, Ireland TN Ireland Full time

Company Overview:

TN Ireland's Global Biostatistics team helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.

We have a collaborative and supportive team environment, where our experts are engaged in the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas.

Job Description:

You will provide experienced technical expertise to develop process methodology for the department to meet internal and external clients' needs.

Key Responsibilities:

  1. Programming and Development:
  2. Plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs.
  3. Perform, plan, co-ordinate and implement the following for complex studies: The programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing.
  4. The programming of analysis datasets (derived datasets) and transfer files for internal and external clients.
  5. The programming quality control checks for the source data and report the data issues periodically.

Required Skills and Qualifications:

  1. 5+ years Statistical Programming experience within the Life Science industry
  2. BSc or MSc degree in Biostatistics or related field
  3. Experience in SAS Base, and good knowledge of SAS graph and SAS Macros
  4. Ability to implement more advanced statistical procedures as per specifications provided by Biostatistician.
  5. Excellent knowledge of CDISC standards (SDTM and ADaM)
  6. Thorough understanding of relational database components and theory
  7. Excellent application development skills
  8. Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.
  9. Ability to work on multiple projects, plan, organize and prioritize activities
  10. Experience as technical team lead directly engaging clients and coordinating tasks within a programming team
  11. In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Benefits:

  1. Global exposure
  2. Variety of therapeutic areas
  3. Collaborative and supportive team environment
  4. Access to cutting-edge and innovative, in-house technology
  5. Excellent career development and progression opportunities
  6. Work-Life Balance, with a strong focus on a positive well-being

Others:

When you join our diverse, global team, you'll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.



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