• Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.
• At least 5 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
• Statistical Programming and SAS hand-on experience
• Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data.
• Good understanding of ICH and regulatory guidelines
• Working knowledge of clinical data and relevant data standards
• Accountable for the quality and timely delivery of datasets and displays required for their clinical study reports as well as other asset level deliverables they may be programming
• Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables
• Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate.
• Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.
• Will be knowledgeable in core safety standards as well as TA standards pertinent to their project, may aid in development of standards necessary for their study
• May contribute to department level initiatives.

  
Work Location Assignment: Flexible
  
Work Location Assignment: Flexible

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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