SAS Clinical Programmer Analyst (Pharma/Biotech) -
Remote EST
Duration – 6 – 12 months
Number or positions – 20
Summary: SAS will provide analytical services in support of customer’s clinical research studies and FDA submission process
QUALIFICATIONS – ESSENTIAL • Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, Business Administration, etc. Healthcare or technology related field. • 4-5+ years of SAS programming experience working with clinical trial data in the Pharmaceutical & Biotech industry. • SAS certifications (Base, Advanced, etc.) are highly desired. • Strong SAS Macro Language experience and knowledge.MAJOR RESPONSIBILTIES/ACTIVITIES: • Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming. • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs). • Production and QC / validation programming. • Generating complex ad-hoc reports utilizing raw data. • Applying strong understanding/experience with Efficacy analysis. • Performing lead duties when called upon. • Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.. • Excellent written and spoken communication skills