Provide comprehensive programming support for clinical trials, including development of programs and analysis datasets
Manage and deliver programming assignments with high quality and within specified timelines
Implement programming standards and ensure compliance with regulatory requirements across projects
Required Qualifications
Bachelor's or Master's Degree in Science, Statistics, Information Technology, or a related field
7 years of experience with a Bachelor's or 6 years with a Master's in a pharmaceutical or clinical research setting
Proficient knowledge of clinical trials, statistical concepts, and regulatory standards
Expert level programming skills in SAS and knowledge of CDISC based e-submission
Strong understanding of SDTM and ADaM standards
Average salary estimate
$0
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$0K
$0K
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