Senior SAS Statistical Programmer - Clinical Trials Lead

Cytel; Columbus (OH); On-site; USD 140,000 - 200,000; Full time

Benefits offered by this job

Equal opportunity employer

Job summary

Cytel is seeking a Principal Statistical Programmer to work embedded with a global pharmaceutical client. You will lead SAS programming for complex clinical trial data and support CDISC SDTM/ADaM submissions with minimal supervision.

The role requires strong leadership, regulatory submission experience, and excellent communication. You will interact with CROs, FDA/EMA, and internal stakeholders, driving quality and timelines.

Qualifications

• MS or BS in biostatistics with pharma experience.
• Experience in SDTM/ADaM data standards and Define.xml.

Responsibilities

• Lead SAS programming for tables, listings and figures for complex clinical trials.
• Ensure SDTM/ADaM datasets and submissions meet regulatory standards.
• Provide expert technical support and project leadership to the team.

Skills

SAS programming

CDISC SDTM/ADaM

Regulatory submissions

Leadership

Clinical programming

SAS macros

BASE SAS

FDA/ICH compliance

Education

MS in biostatistics

BS in biostatistics

Tools

SAS

Job description

Cytel is seeking a Principal Statistical Programmer to work embedded with a global pharmaceutical client. You will lead SAS programming for complex clinical trial data and support CDISC SDTM/ADaM submissions with minimal supervision.

The role requires strong leadership, regulatory submission experience, and excellent communication. You will interact with CROs, FDA/EMA, and internal stakeholders, driving quality and timelines.