Senior SAS Programmer — Remote, CDISC SDTM/ADaM Expert

Cytel; Carson City (NV); Remote; USD 110,000 - 180,000; Full time

Job summary

Cytel is seeking a Senior Statistical Programmer to work with a pharma client, focusing on SAS programming and CDISC SDTM/ADaM standards. This fully remote role supports multiple phase I–IV trials and requires strong data manipulation and analysis skills.

Responsibilities include creating SDTM/ADaM datasets, TLFs, and submission-ready documents, with lead duties as needed. A bachelor’s degree and extensive SAS experience in the pharmaceutical/biotech sector are required, with preference for a

Qualifications

• Bachelor’s degree in Statistics, Computer Science, Mathematics, etc.
• At least 8 years of SAS programming with clinical trial data; 6+ years with a master’s degree
• Experience leading studies; juggling multiple projects preferred
• Strong SAS data manipulation, analysis and reporting skills
• Solid experience with CDISC SDTM/ADaM standards
• Experience with submissions documents and define.xml

Responsibilities

• Perform data manipulation, analysis and reporting of clinical trial data (safety and efficacy) using SAS
• Generate and validate SDTM/ADaM datasets and TLFs
• Produce and QC/validate programming outputs
• Create ad-hoc reports from raw data
• Apply expertise in efficacy analysis
• Prepare submission documents and eCRTs
• Coordinate with cross-functional teams and client on requirements
• Lead when requested
• Collaborate effectively in a globally dispersed team

Skills

SAS programming

CDISC SDTM/ADaM

Data manipulation

Ad-hoc reporting

Lead duties

Cross-functional communication

Education

Bachelor's degree in Statistics/CS/Math

Master's degree (preferred)

Tools

SAS

Job description

Cytel is seeking a Senior Statistical Programmer to work with a pharma client, focusing on SAS programming and CDISC SDTM/ADaM standards. This fully remote role supports multiple phase I–IV trials and requires strong data manipulation and analysis skills.

Responsibilities include creating SDTM/ADaM datasets, TLFs, and submission-ready documents, with lead duties as needed. A bachelor’s degree and extensive SAS experience in the pharmaceutical/biotech sector are required, with preference for a