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Position: Senior Statistical Programmer
Institution: Labcorp Drug Development
Location: Argentina, Brazil, Colombia, Costa Rica, Mexico, Peru
Duties: The Senior Statistical Programmer Performs 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; Mentor programmers in the processes around statistical programming deliverables; Present and share knowledge at department meetings; Continually identify and suggest ways to improve the efficiency, quality and productivity of statistical programming
Requirements: BS in programming, statistics, math, computer science, engineering, computing, public health or related; 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; Knowledge of CDISC requirements; Fluent English
   
Text: Senior Statistical Programmer The Senior Statistical Programmer Performs 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; Mentor programmers in the processes around statistical programming deliverables; Present and share knowledge at department meetings; Continually identify and suggest ways to improve the efficiency, quality and productivity of statistical programming BS in programming, statistics, math, computer science, engineering, computing, public health or related; 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; Knowledge of CDISC requirements; Fluent English
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