The Senior Statistical Programmer is responsible for producing basic analysis displays and information from the

clinical data management database and programing all tables, listings, and graphs necessary for a clinical study

report in accordance with Atorus and/or sponsor standard operating procedures (SOPs), Good Clinical Practice

(GCP), ICH Guidelines and sponsor requirements.

JOB RESPONSIBILITIES

Create and/or quality control (QC) SAS datasets of clinical data from clinical databases; create and/or QC

safety data sets; create efficacy datasets; create project specific macros and formats; load client data from

other platforms and other software packages; prepare data to be sent to clients

Mandatory skill - Hands-on experience with CDISC/SDTM/ADaM programming.

Prepare and/or review documentation describing all datasets and variables within, including derived

variables, and the project as a whole

Perform data checks as needed, to ensure integrity and correctness of data displays. Prepare

documentation for programs

Program and/or QC customized data displays, (including data listings, summary tables and routine

graphics) in accordance with approved statistical analysis plan and shell displays for clinical research

studies. Code is to be written using Base SAS programs, SAS procedures, R, or standardized macros.

Perform data checks as needed to understand structure and content of data

Assume responsibilities for data transfers, including documentation

Act as lead programmer for projects

Handle miscellaneous tasks as assigned by management

QUALIFICATIONS

University degree in computer science or math degree or equivalent.

5+ years clinical programming or SAS programming experience.

Proficiency in at least one of SAS, SAS Macro, R, Python language.

High degree of accuracy and attention to detail.

Some travel required for meetings.

Senior Statistical Programmer

Job Description