Live opening · Posted 3 days ago
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Description supplied by the original job listing.
Job Responsibilities:
Write, modify, and maintain SAS programs for the creation of Analysis Data Set (ADS) and (Tables, Figures, and Listing) TFLs in an efficient manner
Perform program validation and quality control of ADS and TFLs produced by other programmers
Identify the programming issues and fill the issue and action tracking log where applicable.
Update the programming quality control record with programming or QC details.
Provide programming support for data management and data validation as needed.
Understand, execute and improve company SAS macros.
Produce the derived dataset specifications, programming specifications, and other process supporting documents
Learn internal and external Standard Operating Procedures (SOPs)/ Working Practice
Documents WPDs, International Council for Harmonisation - Good Clinical Practice (ICH-GCP) and/or other international/local regulatory requirements.
Ensure all statistical activities in accordance with internal and external quality standards, SOPs/WPDs, ICH-GCP and/or other international/local regulatory requirements.
Improve technical skills including SAS programming, statistics and clinical trial through self-learning, coaching, internal training, external training, and on-job training, etc.
Develop effective team communication and team work.
Proactively participate in process/quality improvement initiatives.
Qualification:
Bachelor degree or above in Statistics, Mathematics, Computer Science, or related fields (e.g., Bioinformatics, Biostatistics, Public Health, etc.)
Basic SAS programming skill
Fresh graduates are acceptable. Relevant practical experience in SAS programming is preferred (no industry restrictions)
Good communication skills, including ability to communicate in English verbally and in writing.
Work arrangement
Yes
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