Bachelors degree in Statistics, Biostatistics, Life Sciences, Biotechnology, Computer Science, Pharmaceutics, Pharmaceutical Chemistry, Pharmacy, Computer and Information Systems Engineering, Regulatory Affairs or a related field or foreign degree equivalent; and 8 years of progressive, postbaccalaureate experience performing SAS programming in the biotech, pharmaceutical, health care or medical device industry, performing all work in compliance with applicable regulations. Must also include 6 years of experience in performing statistical programming using SAS for creating and testing Analysis Datasets, Tables, Listings and Figures for Phase IIV clinical studies; 3 years of experience in writing SAS Macros; 3 years of experience overseeing Statistical Programming projects; 2 years of experience with oncology clinical studies; 3 years of experience implementing CDISC standards; and 1 year of experience with regulatory submissions including BLA, NDA, NDS, and MAA.br br Employer will accept a Masters degree in Statistics, Biostatistics, Life Sciences, Biotechnology, Computer Science, Pharmaceutics, Pharmaceutical Chemistry, Pharmacy, Computer and Information Systems Engineering, Regulatory Affairs or a related field or foreign degree equivalent; and 6 years of experience performing SAS programming in the biotech, pharmaceutical, health care or medical device industry, performing all work in compliance with applicable regulations in lieu of a Bachelors degree and 8 years of experience. Experience may be gained concurrently. Any suitable combination of education, training or experience is acceptable.br br Telecommuting from anywhere in the US is permitted

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