Requires a Masters Degree or foreign equivalent in Statistics, Computer Science, Mathematics, or a related field and 3 years of programming experience in processing clinical trial data in the biotechnology, pharmaceutical or health related industry. Must have experience in Interpreting, modifying, and adapting procedures, practices, and methods, in accordance with existing policies and standards for application to specific problems or tasks; SAS, Base, Stat, Macro, and graph programming in a clinical data environment; Creation of current CDISC data structures; Relational database structure and understanding reporting systems; Implementing of standardization methodology; Supporting study requirements with challenging timelines under direct supervision by a programming lead; Pharmaceutical clinical development i.e. understanding safety deliverables, efficacy analysis and providing programming support needs for BLA and other regulatory submissions; Project management with supervision; Development and execution of user requirements, validation plans, and operational and performance protocols.br br Per Executive Order, Regeneron requires all U.S. employees to be fully vaccinated against COVID19, unless they are legally entitled to an accommodation for medical or religious reasons.
Categories: eb3
0 Comments