Statistical Programmer

Position: Statistical Programmer
Department: Biostatistics, Data Management and Medical Writing
Direct Manager: Head of Statistics, Data Management and Medical Writing
Location: Prague Czech Republic
Employment type: Full time employment

Position Summary:

Responsible for statistical programming aspects of individual clinical trials as assigned by the Head of Department.

Key Activities and Responsibilities:

  • Contribute to statistical programming tasks regarding the assigned clinical trials as well as at the project level. These tasks include: production of datasets and TFLs, creating macros, validations, proper documentation, input to statistical analysis plan, operational aspects regarding producing the statistical reporting for clinical trials
  • Ensure compliance with regulatory requirements, including appropriate reflection of guidelines regarding clinical trial analysis and reporting, implementation of standards such as CDISC, etc.
  • Support and provide input to biostatistics, medical writing and data management as required
  • Ensure timeliness and quality of assigned deliverables
  • Establish and maintain sound working relationships and effective communication with other functions/departments

Competences, Skills and Qualification:

  • At least a B.Sc. in Life Science or Computer Science
  • Demonstrated professional experience as a SAS Programmer (operational knowledge of SAS software, with preferably SAS base and advanced certification)
  • Experience in statistical reporting for clinical trials
  • Previous experience in the pharmaceutical industry, i.e. sponsor or CRO is preferred
  • Knowledge of basic statistical methods and data management
  • Knowledge of regulatory guidelines, requirements and standards (GCP, ICH, CDISC)
  • Organized, with structured thinking and ability to understand complex data
  • Fluent English and good communication skills

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