Pfizer, Inc.
Chennai, Tamil Nadu, India
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...