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Position: Senior Statistical Programmer
Institution: Labcorp Drug Development
Location: Japan
Duties: Perform the role of the Lead Statistical Programmer; Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and the client, etc; Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs; Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated eCRFs and Reviewers Guides to support SDTMs and ADaMs; Develop specifications for SDTMs and ADaM datasets
Requirements: Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects; Typically 3 - 5 years of SAS® programming experience in the CRO or Pharmaceutical industry, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job; Previous Lead experience as a Statistical Programmer within a biotech, CRO or pharma company; Excellent organizational, time management and project management skills with team leadership experience, as demonstrated by ability to organize and motivate project teams and the ability to delegate and prioritize work to meet project timelines
   
Text: Senior Statistical Programmer Perform the role of the Lead Statistical Programmer; Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and the client, etc; Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs; Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated eCRFs and Reviewers Guides to support SDTMs and ADaMs; Develop specifications for SDTMs and ADaM datasets Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects; Typically 3 - 5 years of SAS® programming experience in the CRO or Pharmaceutical industry, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job; Previous Lead experience as a Statistical Programmer within a biotech, CRO or pharma company; Excellent organizational, time management and project management skills with team leadership experience, as demonstrated by ability to organize and motivate project teams and the ability to delegate and prioritize work to meet project timelines
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