Job Details

Deliver statistical programming expertise for clinical studies with lower complexity. Ensure accurate data analysis, reporting, & adherence to regulatory standards. Develop SAS programs for generating A - Da. M datasets, tables, listings, & figures. Create specifications for A - Da. M datasets for individual & integrated analyses. Collaborate closely with crossfunctional teams to achieve project objectives. Prepare documentation for regulatory submissions, including reviewers guides & data definition documents. Lead development of standard SAS macros & participate in development of standard operating procedures. Provide supervision & mentorship to statistical programmers & analysts. Qualifications. Education & Experience. Must have a MS in statistics, biostatistics, computer science, mechanical engineering or a related field & 2 years as a statistical analyst leading statistical programming activities for clinical studies. Of experience required, must have 2 years:applying SAS programm...Analyst, Mechanical Engineer, Computer Science, Senior, Clinical, Technology, Program