Kijiji Jobs Toronto Full Time

Programmers & Computer in City of Toronto

Sr Statistical Programmer

Description

Job Description:
The Statistical Programmer will be responsible for providing hands-on data analysis support in clinical project teams. This individual will participate in the design, development, documentation, and quality control process for SAS programs used to access, extract, transform, review, analyze, and submit clinical data and analysis results for studies. This individual will participate in departmental and cross functional technology development and process improvement activities.
Key Responsibilities:
Utilize SAS to generate and validate tables, listings, and figures (TLF) based on SAPUse major statistical programming language to perform data analysis for various needsProvide statistical analysis support for post approval studiesEvaluate and ensure CDISC compliance of study tabulation and analysis data filesWrite specifications and statistical programs to generate analysis datasets and outputsPerform data analysis tasks with minimal supervisionProvide programming support for data managementDevelop statistical toolbox for advanced data modelling, tabulation, and visualizationParticipate in reviewing and validating data analysis results
Qualification:
Strong SAS programing skill in producing various types of outputs such as TLFs and datasets with minimum of 3 years of experiencesExtensive statistical programming experience in producing deliverables either on scheduled or adhoc basisBS degree in Statistics, Mathematics, Computer Science, or related field, MS in Statistics or Biostatistics is preferredExperience with producing outputs submitted to the FDA and other regulatory agenciesExcellent organizational skill to prioritize multiple tasks and goals to ensure timely completionAttention to detail and able to adapt to a fast-paced environmentAbility to work both independently and in a cross-functional teamExcellent communication skillsSufficient knowledge in CDISC and SDTM/ADAM for FDA submission complianceAdequate knowledge in clinical trial research methodology, ICH, GCP and regulationsExperiences in medical device and cardiovascular disease is desirable, but not required

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