Principal Statistical Data Scientist - Chennai, India - Pfizer

Description

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 experienceClinical trials expertise with an understanding of data operations required for the reporting of clinical trial data.

Good understanding of ICH and regulatory guidelinesWorking knowledge of clinical data and relevant data standardsAccountable 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 programmingEnsures appropriate documentation and QC across the lifespan of the study for all of their programming deliverablesExhibits 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 studyMay contribute to department level initiatives.

Work Location Assignment:

FlexibleWork Location Assignment:

FlexiblePfizer 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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