Job Description

\xc2\xb7 A productive, hands-on programmer who applies technical knowledge and practical experience to deliver statistical programming deliverables to support assets and study teams with limited supervision early in role and independently later in role.\xc2\xb7 Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures for which they are responsible\xc2\xb7 Ensures adherence to high quality programming standards in their daily work.JOB RESPONSIBILITIES\xc2\xb7 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\xc2\xb7 Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables\xc2\xb7 Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate.\xc2\xb7 Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.\xc2\xb7 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.\xc2\xb7 May contribute to department level initiativesQUALIFICATIONS / SKILLS\xc2\xb7 Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.\xc2\xb7 At least 6-8 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.\xc2\xb7 Statistical Programming and SAS hand-on experience.\xc2\xb7 Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data.\xc2\xb7 Good understanding of ICH and regulatory guidelines\xc2\xb7 Working knowledge of clinical data and relevant data standards\xc2\xb7 Strong written and oral communication skills, and project management skills\xc2\xb7 Proven ability to operate with limited oversight\xc2\xb7 Knowledge of at least 1 Therapeutic Area\xc2\xb7 Proven ability to manage delivery under tight timelines.\xc2\xb7 CDISC experience desirablePfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Medical#LI-PFE

Pfizer