Careers

 •Act as a Lead SAS Programmer in guiding team and doing all Project deliverables.

 •Write complex SAS programs to generate tables, listings and figures for inclusion in Clinical Study       Reports, annual safety reports, and other documents, as requested.

 •Participate in the clinical trials process by reviewing CRFs, edit check specifications, mock tables/listings/figures, etc

 •Also had experience with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data.

 •Involved in creation of ADHOC reports for FDA, MAA and PMDA Submission Agencies.

 •Assist with statistical quality assurance review and program validation for each project.

 •Interact with other departments such as Statisticians, Project Management, Data Management, Clinical, Regulatory and Medical Writer teams to ensure a high level of client satisfaction through successful execution of projects.

Qualification:

This position requires a minimum of a Bachelor’s Degree in Statistics, Computer Science, Information Technology, Management Information Systems or a combination of education and experience equating to the U.S. equivalent of a bachelor’s degree in one of the aforementioned subjects.