Employer Active
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:
Bachelor's degree in a technical field such as Statistics, Mathematics, Computer Science or related field with 4 years of experience
Masters's 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