Principal SAS Programmer

Artmac; India; On-site; INR 4,000,000 - 6,000,000; Full time

Job summary

Artmac Soft is seeking a Principal SAS Programmer for a remote, full-time role. The candidate should have 10+ years of SAS programming experience in the clinical domain and strong end-to-end programming skills.

Responsibilities include ADaM dataset development, TLF creation, regulatory submission support, and QC of outputs. Strong SAS Base, macros, and data manipulation are required; R knowledge is a plus.

Qualifications

• Bachelor's degree or equivalent combination of education and experience.

Responsibilities

• Lead end-to-end SAS programming activities for clinical trials.
• Develop, validate, and maintain SAS programs for analysis and reporting.
• Design, create, and validate ADaM datasets per CDISC standards.
• Develop Tables, Listings, and Figures (TLFs) for studies.
• Support clinical efficacy programming and regulatory submissions.
• Review specifications, datasets, and outputs for accuracy.
• Perform independent programming validation and QC.
• Troubleshoot complex SAS programming/data issues.

Skills

SAS programming

ADaM datasets

CDISC (ADaM/SDTM)

SAS Base programming

Regulatory submissions

R programming

Education

Bachelor's degree or equivalent

Tools

SAS Studio

Job description

Who We Are

Artmac Soft is a technology consulting and service-oriented IT company that provides innovative technology solutions and services to customers.

Job Description

Job Title : Principal SAS Programmer

Job Type : Full-Time

Experience : 10+ Years

Location : Remote

Responsibilities

• 10+ years of professional experience in SAS programming in the Clinical domain.
• Strong end-to-end SAS programming experience is mandatory.
• Hands-on experience with ADaM dataset development and programming is required.
• Experience developing clinical study TLFs using SAS.
• Strong experience in SAS Base programming, including DATA steps, PROC SQL, macros, and data manipulation.
• Experience with R programming is a plus.
• Experience supporting clinical efficacy programming.
• Strong knowledge of SAS Base programming and advanced SAS techniques.
• Strong understanding of clinical trial data and statistical programming processes.
• Knowledge of CDISC standards, particularly ADaM; SDTM knowledge is beneficial.
• Lead and perform end-to-end SAS programming activities for clinical trials.
• Develop, validate, and maintain SAS programs for clinical data analysis and reporting.
• Design, create, and validate ADaM datasets in accordance with CDISC standards.
• Work with clinical study data from SDTM/clinical databases through ADaM and analysis outputs.
• Develop and validate Tables, Listings, and Figures (TLFs) for clinical studies.
• Perform programming activities supporting clinical study analysis and regulatory submissions.
• Review specifications, datasets, programming requirements, and analysis outputs for accuracy and completeness.
• Conduct independent programming validation and QC of datasets and statistical outputs.
• Troubleshoot complex SAS programming and data-related issues.

Qualification

• Bachelor's degree or equivalent combination of education and experience.