Principal statistical programmer
1 month ago
Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.
· 6 + 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 · Strong written and oral communication skills, and project management skills · Proven ability to operate with limited oversight · Knowledge of at least 1 Therapeutic Area · Proven ability to manage delivery under tight timelines.
· CDISC experience desirable
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