TL;DR

Statistical Programmer/Analyst III: Analyzing data and reporting statistical results in the pharmaceutical, biotechnology, medical device, and consumer health industries with an accent on CDISC standards and FDA submissions. Focus on developing and maintaining SAS programs and macros to create Tables, Listings, and Graphs for Clinical Study Reports.

Company

%hirify_global% is a global full-service CRO specializing in clinical development and functional solutions.

What you will do

Analyze data and report statistical results.
Develop SDTM and ADaM analysis data specifications for programming.
Develop, debug, and maintain SAS programs and macros to create Tables, Listings and Graphs for Clinical Study Report.
Implement SAS programs to generate Define-XML package for FDA submission.
Implement statistical data analysis and communicate with statisticians for statistical input.

Requirements

Bachelor’s/Master’s degree in Statistics, Mathematics, Computer Science, Electrical Engineering, Biotechnology or related scientific disciplines with 2+ years of statistical programming experience required.
Proven knowledge and training in high level computing languages such as SAS, C/C++, Java, R, Python, MATLAB and SQL.
Working knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.
Detail oriented and ability to learn and adapt to changes.

Culture & Benefits

Flexible Working Hours
Full performance and development process with end of year reviews
Team events and end of year party
Employee satisfaction survey - your feedback is important for continuous improvement
Health Insurance