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SAS programmer experience in Med Device or pharma REQUIRED
Job Responsibilities:
Develop complex analysis datasets specifications and summary output (tables listings or graphs) for inclusion in clinical reports or presentations; Create complex programs that meet regulatory and company
standards to permit efficient programming reporting and review utilizing statistical programming languages (e.g SAS)
Review and validate statistical programs and ensure that all appropriate program validation documentation to meet regulatory and company standards are consistently structured to permit efficient programming reporting and review
Perform complex analysis in response to data requests in collaboration with designated statistician
Collaborate with CDM (Clinical Data Management) and designated statistician to review draft CRFs (Case Report Forms) database specifications and perform edit checks
Qualifications:
Bachelors degree in a technical field such as Statistics Mathematics Computer Science or related field with 4 years of experience
Masterss degree in a technical field such as Statistics Mathematics Computer Science or related field with 2 years of experience
Previous statistical programming experience (e.g. SAS)
Full Time