Provide comprehensive programming support for clinical trials, including development of programs and analysis datasets
Manage and deliver assignments with quality and within timelines, ensuring compliance with regulatory requirements
Standardize deliverables across study projects and communicate programming deliverables' status and resource gaps
Required Qualifications
Bachelor's or Master's Degree in Science, Statistics, Information Technology or equivalent
7+ years of professional experience in a pharmaceutical or clinical research setting as a programmer
Proficient knowledge of clinical trials, drug development processes, and statistical concepts
Strong understanding of SDTM and ADaM standards
Demonstrated proficiency in using SAS for analysis datasets and TLGs
Average salary estimate
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