Clinical Application Specialist III – SAS_ADaM Programming_35706

K3-Innovations, Inc.; United States; Remote; USD 110,000 - 160,000; Full time

Job summary

K3-Innovations, Inc. is seeking an experienced SAS Programmer with strong CDISC, ADaM, and TLF expertise to support safety and efficacy analyses for Immunology projects.

The role involves data analysis, ADaM dataset development, and collaboration with statisticians in a clinical research setting. The ideal candidate will have extensive experience translating aCRF and SDTM data into ADaM specifications, building and validating ADaM datasets, and producing high-quality TLF outputs while adhering

Qualifications

• 6–8+ years of SAS programming experience in clinical trial data analysis.
• 8+ years of ADaM and TLF programming experience for safety and efficacy analyses.
• Strong knowledge of CDISC standards.

Responsibilities

• Support safety and efficacy analyses for Immunology projects.
• Interpret aCRF and SDTM data, SAP, and SPP to develop ADaM specifications and datasets.
• Develop and validate ADaM datasets and TLF outputs.
• Create, develop, and validate TLF (Tables, Listings, and Figures) outputs.
• Apply CDISC standards to support clinical trial analyses.
• Learn and apply internal macros and processes.
• Collaborate with statistical programmers and statisticians on deliverables.

Skills

SAS programming

ADaM

TLF

CDISC standards

SAS Studio

Immunology domain

Job description

Are you an experienced SAS Programmer with strong CDISC, ADaM, and TLF programming expertise? We’re seeking a skilled clinical programming professional to support safety and efficacy analyses for Immunology projects.

This is an excellent opportunity for an experienced programmer to contribute to clinical trial data analysis, develop and validate ADaM datasets, and collaborate with statistical programmers and statisticians in a clinical research environment.

• Support safety and efficacy analyses for Immunology projects.
• Interpret aCRF, SDTM data, SAP, and SPP information to develop ADaM specifications and datasets.
• Support the creation, development, and validation of ADaM datasets.
• Develop and review TLF (Tables, Listings, and Figures) outputs.
• Apply CDISC standards and clinical programming expertise to support clinical trial analyses.
• Learn and apply internal programming macros and processes.
• Collaborate with statistical programmers and statisticians to support project deliverables.

Required Qualifications

• 6–8+ years of SAS programming experience supporting clinical trial data analysis.
• 8+ years of ADaM and TLF programming experience supporting safety and efficacy analyses.
• Strong knowledge of CDISC standards.
• Proven experience translating aCRF, SDTM data, SAP, and SPP into ADaM specifications.
• Hands‑on experience supporting ADaM programming and reviewing TLF outputs.
• Ability to quickly learn internal macros, tools, and processes.
• Strong communication skills and a collaborative, team-oriented approach.
• Experience with SAS Studio or SAS Enterprise Guide.
• Clinical experience.
• Immunology therapeutic‑area experience is preferred but not required.

Ideal Candidate: An experienced clinical SAS programmer with deep ADaM and TLF expertise, a strong understanding of CDISC standards, and the ability to support high-quality clinical trial safety and efficacy analyses.

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