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Position: Clinical SAS Programmer
Institution: Phastar
Location: Canada, Germany, United Kingdom, United States
Duties: Act as lead programmer for SDTM creation; Create and develop SDTM programs and datasets; Program complex safety/efficacy datasets; Develop and debug more complex macros; Create, QC and update complex dataset specifications (including efficacy) for single or multiple studies; Review simple study design SAP with supervision; Review listings and simple summary shells without supervision and provide feedback; Utilise your awareness of CDISC SDTM and ADaM implementation guidelines
Requirements: BSc, MSc or PhD in computer science, mathematics or a science related discipline; Excellent and extensive knowledge of CDISC SDTM and ADaM standards and application; Substantial SAS programming experience within the pharmaceutical industry; Proficiency in macro development and safety and efficacy datasets; Familiarity with GCP and regulatory requirements; Excellent written and verbal communication skills
   
Text: Clinical SAS Programmer Act as lead programmer for SDTM creation; Create and develop SDTM programs and datasets; Program complex safety/efficacy datasets; Develop and debug more complex macros; Create, QC and update complex dataset specifications (including efficacy) for single or multiple studies; Review simple study design SAP with supervision; Review listings and simple summary shells without supervision and provide feedback; Utilise your awareness of CDISC SDTM and ADaM implementation guidelines BSc, MSc or PhD in computer science, mathematics or a science related discipline; Excellent and extensive knowledge of CDISC SDTM and ADaM standards and application; Substantial SAS programming experience within the pharmaceutical industry; Proficiency in macro development and safety and efficacy datasets; Familiarity with GCP and regulatory requirements; Excellent written and verbal communication skills
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