Senior Scientist, Statistical Programming
On-site · North Wales, Pennsylvania, United States
Job Summary
Senior Scientist, Statistical Programming responsible for supporting statistical programming activities for clinical trial data analysis, developing SAS programs to create ADaM datasets and TFLs for regulatory submissions, collaborating with biostatisticians and project leads, ensuring CDISC/ICH standards, and coordinating a global programming team; requires advanced degree with extensive experience in SAS, CDISC standards, and clinical trial programming.
Required Qualifications
- Master’s degree or equivalent in Computer Science, Statistics, Applied Mathematics, Biomedical Engineering, or a closely related field and 3 years of experience in the position offered or a related role; OR a Bachelor's degree or equivalent in Computer Science, Statistics, Applied Mathematics, Biomedical Engineering, or a closely related field and 5 years of experience in the position offered or a related role.
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