What you will be doing :
Develops SAS programs to generate listings, tables and figures as outlined by mock TLF shells
· Performs quality control (source code review, double-programming and log review) of SAS programs
· Develops SAS programs to generate CDISC and other analysis data sets as outlined by respective specifications
· Prepares specifications for CDISC and other analysis data sets
· Assists Data Management with SAS programming needs
· Acts as Lead Biostatistical Programmer to interact with the Lead Biostatistician and the study team
· Develops and validates general SAS macros
EDUCATION, SKILLS & COMPETENCIES:
Educational Background
· BS or equivalent from accredited college or university, in statistics, IT, mathematics or closely related field or work related experience to be able to perform this role
Experience
· 4-6 years of experience in SAS programming within the area of clinical trials.
· Prior experience using computerized information systems preferred.
· Knowledge of ICH and local regulatory authority drug research and development regulations preferred.
Apply here: https://premier-research.com/our-company/careers/?jobID=oYjJsfwc&locations=India