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JOB SUMMARY<ul><li>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.</li><li>Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures for which they are responsible.</li><li>Ensures adherence to high quality statistical data sciences principles, processes and techniques in their daily work.</li></ul>JOB RESPONSIBILITIES<ul><li>Indicate the primary responsibilities critical to the job.</li><li>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.</li><li>Ensures appropriate documentation and QC across the lifespan of the study for all of their programming.</li><li>Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate.</li><li>Works with statisticians and statistical data sciences to ensure clear specifications for their programmed deliverables are in place.</li><li>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.</li><li>May contribute to department level initiatives.</li></ul>QUALIFICATIONS / SKILLS<ul><li>Bachelor or Master (preferred) Degree in Statistics, Data Sciences, Biological Sciences, IT, or related field.</li><li>At least 3 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.</li><li>Statistical Programming and SAS, R, or Python hands-on experience.</li><li>Familiarity with R packages, Shiny Apps, Markdown reports and other associated data science and data analytics tools and AI/ML highly desired.</li><li>Experience with Real World Evidence and other big data sources and associated standards (e.g., OMOP, JSON, ODHSI) in support of regulatory filings desired.</li><li>Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data.</li><li>Good understanding of ICH and regulatory guidelines.</li><li>Working knowledge of clinical data and relevant data standards.</li><li>Strong written and oral communication skills, and project management skills.</li><li>Proven ability to operate with limited oversight.</li><li>Knowledge of at least 1 Therapeutic Area.</li><li>Proven ability to manage delivery under tight timelines.</li><li>CDISC experience desirable.</li></ul>&nbsp;&nbsp;Please apply by sending your CV and a motivational letter in English.

Senior Associate, Senior Statistical Data Scientist

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senior associate, senior statistical data scientist

Pfizer Hellas