SAS Programmer (with the focus on clinical trial regulatory submission work)
Location: Boston, MA or Amherst, NY
In this role, you’ll support statisticians by using SAS in a UNIX environment to create, develop, maintain, and validate SAS programs for a variety of applications, with a primary focus on clinical trial regulatory submissions. The work includes generating database queries; creating analysis datasets, tables, graphics, and metadata files adhering to CDISC ADaM standards; and maintaining and validating standard macros and programs. You’ll have the opportunity to contribute to a variety of projects and showcase your SAS capabilities in a growing and collaborative department.
We are looking for candidates with a degree in a quantitative or scientific field (such as mathematics or statistics); some year(s) of professional work experience in clinical research or pharma programming using SAS, preferably in a UNIX environment; experience with ADaM programming and SAS macro language, ODS graphics, and proc sql; and excellent communication skills (both written and verbal).
To apply: Send your resume, cover letter, and sample SAS code (written entirely by you). If you are interested in working in our Boston, MA office, send this material to email@example.com.
If you are interested in working in our Amherst, NY office, send your materials to firstname.lastname@example.org.
All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, national origin, disability, or veteran status.