Apply on Employer Site

Ecocareers · 2 months ago

Senior Statistical Programmer II

Boston, MA

Full-time

Onsite

Senior Level

5+ years exp

Confidential company is seeking a Senior Statistical Programmer II to analyze and report complex clinical trial data. The role involves coding complex SAS programs, performing quality control checks, and creating CDISC data sets while ensuring high quality standards in a team environment.

Staffing & Recruiting

Responsibilities

Codes complex SAS programs (including Macro language, SAS/STAT and SAS/GRAPH) for applications designed to analyze and report complex clinical trial data and for electronic review, exchange, transformation, and submission of data in CDlSC SDTM format; consistently meeting objectives of the study

Performs quality control checks of SAS code and output produced by other Statistical Programmers

Demonstrates proficient knowledge of clinical development and medical data

Solves clinical trial reporting problems and has a proven technical proficiency in supporting daily operations and ensuring that project tasks are completed accurately with limited supervision

Creates CDISC data sets by transforming various raw data sources, including different Electronic Data Capture (EDC) databases and Interactive Web Response Systems (IWRS), tables, figures, and listings reporting and submitting the results of clinical trials for investigational medications

Works with all types of coding dictionaries (MedDRA and WHODD) commonly used by the pharmaceutical industry

Works in a team environment providing technical leadership and solving clinical trial reporting problems within budget and customary timeline constraints while assuring high quality standards