Senior Statistical Programmer: SAS, CDISC, Regulatory

Real Staffing; Irvine (CA); Hybrid; USD 85,000 - 121,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Job summary

Medical Device Company in Irvine, CA is seeking a Senior Statistical Programmer Contractor to provide hands-on SAS programming support for clinical studies. You will develop and validate analysis datasets and regulatory outputs with strong independence, and work on cross-functional collaborations.

The role is onsite 3–4 days per week. The position requires 8+ years of relevant experience (or 6+ with a Master's), deep SAS expertise, and familiarity with CDISC SDTM/ADaM, GCP, and regulatory

Qualifications

• Bachelor's degree with 8+ years of relevant experience or Master's with 6+ years of experience.
• Strong SAS programming expertise including SAS Base, SAS/STAT, and SAS Macros.
• Experience with CDISC SDTM and ADaM standards and regulatory submissions.

Responsibilities

• Develop and validate analysis datasets, specifications, and outputs (tables, listings, figures) for clinical study reports and regulatory submissions.
• Create, maintain, and enhance SAS programs for reporting and traceability; ensure accuracy and inspection readiness.
• Support planned and ad-hoc analyses, respond to data review questions, and collaborate with cross-functional teams on CRFs, database specs, and data derivations.

Skills

SAS

SAS Base

STAT

SAS Macros

CDISC

ADaM

SDTM

clinical trials

Education

Bachelor's degree in Statistics/Mathematics/Computer Science

Master's degree in related field

Job description

Medical Device Company in Irvine, CA is seeking a Senior Statistical Programmer Contractor to provide hands-on SAS programming support for clinical studies. You will develop and validate analysis datasets and regulatory outputs with strong independence, and work on cross-functional collaborations.

The role is onsite 3–4 days per week. The position requires 8+ years of relevant experience (or 6+ with a Master's), deep SAS expertise, and familiarity with CDISC SDTM/ADaM, GCP, and regulatory