at Incyte Corporation in Wilmington, Delaware, United States
Job Description
Responsible for processing clinical data required for statistical analysis of Phase I through III clinical trials, and leading project teams. Function as a lead biostatistical programmer for a compound or a group of studies. Maintain the overall timeline for his/her studies. Maintain the programming standards for his/her studies. Review standard macros used; Review standard datasets used. Discuss need for programming resources for their group of studies. Mentor and train junior programmers on Incyte systems and standards as they work on studies within their area. Assist junior programmers in new study set-up to help identify similar studies. Review Production area after study programming is complete to make sure datasets, programs, and outputs are properly stored. Check that the validation summary reports are clean of errors and warnings and show proper documentation of SAS programs. Review individual study CDISC validation output. Act as a Programming lead for a submission project under supervision of Programming management. Serve as a mentor to junior programmers and as an expert to provide recommendations and solutions to complex problems.
EDUCATION & EXPERIENCE: Master’s degree or foreign equivalent in Statistics, Biostatistics, Computer Science, or related field, and 3 years of related experience. Will also accept a Bachelor’s degree or foreign equivalent in Statistics, Biostatistics, Computer Science, or related field, followed by 5 years of progressive, related experience in lieu of a master’s degree or foreign equivalent in Statistics, Computer Science, or related field and 3 years of related experience.
HOW TO APPLY: Email resume to aguntz@incyte.com. Must reference job title and job PBP-CL in the subject line.
