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| CAREERS - CURRENT OPENINGS |
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| • SAS Programmers |
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Roles and Responsibilities |
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Provide SAS programming support on design, conduct & analysis of clinical trials
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| Provide statistical/programming inputs for CRF design and review |
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Develop programs for generating randomization lists
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| Prepare for edit checks, data review, coding and validation |
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Develop and validate standard / ad-hoc SAS macros
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Generate statistical analysis data sets
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Perform data analysis and assist in report preparation
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Generate data listings, tables and graphs
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Develop programs for quality control of analysis programs
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Set up data transfer programs
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Develop test data files & algorithms
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Provide SAS training to junior SAS programmers and statisticians
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Understand and comply with all SOPs
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Skills & Knowledge Required |
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B.E., B.Tech, or Degree in Statistics or MSc (Maths)
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1-3 yrs of SAS programming experience supporting clinical trial projects.
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More than 3 yrs of statistical experience in other relevant industry
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| Knowledge of clinical trial protocols and pharma domain |
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Strong analytical and logical skills
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Excellent validation and documentation skills
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Experience in extracting data from databases and creating analysis files.
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Excellent organizational, communication, and interpersonal skills
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Enthusiastic and innovative
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Ability to work in teams and dynamic environment
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If you fit the above criteria and interested to work with us please have your CVs emailed to careers@ecronacunova.com |