Remote SAS Statistics Programmer - ADaM/SDTM Expert

Collabera; North Chicago (IL); Remote; USD 83,000 - 96,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Paid parking/public transportation

Paid time off

Job summary

Collabera is seeking an experienced Statistical Programmer to support clinical trial safety and efficacy analyses with hands-on SAS programming and ADaM dataset development. Strong CDISC ADaM/SDTM knowledge and ability to interpret study documentation are essential for producing tables, listings and figures.

The role involves collaboration with statisticians and other programmers to deliver accurate analysis outputs and contribute to regulatory submissions.

Qualifications

• 6 to 8 or more years of SAS programming experience supporting clinical trials.
• Strong hands on experience developing ADaM datasets and specifications.
• Experience interpreting Statistical Analysis Plans and translating requirements into programming deliverables.
• 8 or more years of ADaM and TLF programming experience as specified in the job requirements.
• Experience generating clinical Tables, Listings and Figures for safety and efficacy analyses.

Responsibilities

• Interpret annotated CRFs, SDTM data, SAPs to develop ADaM specifications and datasets.
• Develop and support ADaM programming for clinical trial analyses.
• Create, validate, review ADaM datasets per CDISC standards.
• Generate and review Tables, Listings and Figures supporting safety and efficacy analyses.
• Support clinical trial data analysis and reporting activities.
• Collaborate with statistical programmers and statisticians to deliver outputs.
• Learn and apply internal macros, standards, and processes.

Skills

SAS programming

ADaM datasets

ADaM specifications

CDISC standards

Clinical trial programming

Data analysis

Education

Master's degree in Statistics

Tools

SAS Studio

SAS Enterprise Guide

Job description

Collabera is seeking an experienced Statistical Programmer to support clinical trial safety and efficacy analyses with hands-on SAS programming and ADaM dataset development. Strong CDISC ADaM/SDTM knowledge and ability to interpret study documentation are essential for producing tables, listings and figures.

The role involves collaboration with statisticians and other programmers to deliver accurate analysis outputs and contribute to regulatory submissions.