Senior SAS Programmer - Clinical Trials & ADaM Lead

Oxford Global Resources; Houston (TX); On-site; USD 81,000 - 106,000; Full time

Benefits offered by this job

401(k) Retirement Savings Plan

Supplemental medical benefits

Paid holidays & sick leave

Job summary

Oxford Global Resources in Houston is seeking a SAS Programmer to support clinical studies and regulatory submissions. You will develop and validate SAS programs for analysis datasets, tables, figures, and listings under supervision.

The role requires 2–5 years of related experience, strong SAS skills, and CDISC ADaM knowledge. You will collaborate with sponsors and cross-functional teams, document procedures, and contribute to high-quality deliverables.

Qualifications

• Bachelor's degree required; advanced degree desirable.
• 2–5 years related experience or advanced degree.
• Strong SAS programming and CDISC ADaM knowledge.
• Excellent organizational and communication skills.
• Ability to lead programming teams.

Responsibilities

• Assist with SAS programming for analysis datasets and submissions.
• Develop expertise in writing and validating SAS programs.
• Work with project teams and escalate issues as needed.
• Document programming procedures and coding.
• Lead programming teams and collaborate with Sponsors.

Skills

SAS programming

Statistical analysis

Data manipulation

Macro language

Education

Bachelor's degree

Advanced degree desirable

Tools

CDISC ADaM

Job description

Oxford Global Resources in Houston is seeking a SAS Programmer to support clinical studies and regulatory submissions. You will develop and validate SAS programs for analysis datasets, tables, figures, and listings under supervision.

The role requires 2–5 years of related experience, strong SAS skills, and CDISC ADaM knowledge. You will collaborate with sponsors and cross-functional teams, document procedures, and contribute to high-quality deliverables.