SAS Programmer (with the focus on clinical trial regulatory submission work)
Location: Boston, MA
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).
Entry-level salary is $65,000 per year.
To apply: Send your resume, cover letter, and sample SAS code (written entirely by you) to email@example.com and include SAS202002 in the subject line.
All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, national origin, disability, or veteran status.