Senior Statistical Programmer & Study Lead (SAS)

Syneos Health; Massachusetts; On-site; USD 81,000 - 145,000; Full time

Benefits offered by this job

Company car / car allowance

Health benefits

401k match

Employee stock purchase plan

Bonuses / commissions

Paid time off

Job summary

Syneos Health in the United States seeks a Principal Statistical Programmer for Sponsor Dedicated roles. You will lead programming for a portfolio of studies, manage timelines, and ensure CDISC standards and regulatory compliance across submissions.

This senior role requires 8+ years of SAS/Base/Macro/GRAPH programming in biopharma or CRO environments, mentoring junior programmers, and collaborating with cross-functional teams to deliver high-quality results.

Qualifications

• BA/BS degree required; MS in statistics or computer science desired.
• Minimum 8 years of programming experience using SAS/Base/Macro/GRAPH in biopharma/CRO.
• Data Management experience including CDISC standards is highly desirable.
• Strong SAS programming skills with attention to detail.
• Knowledge of regulatory guidelines and electronic submission standards.

Responsibilities

• Lead as Programming lead for a submission project under supervision of Programming management.
• Mentor/Train junior programmers on Incyte systems and standards.
• Maintain timelines and programming standards for studies.
• Review datasets, macros, and outputs; ensure proper storage and documentation.
• Collaborate with cross-functional teams to plan resources and study setup.

Skills

SAS programming

CDISC standards

Mentoring junior programmers

Project coordination

Biopharma/CRO experience

Education

BA/BS degree

MS in statistics or computer sciences

Tools

SAS Suite (Base/Macro/GRAPH)

Job description

Syneos Health in the United States seeks a Principal Statistical Programmer for Sponsor Dedicated roles. You will lead programming for a portfolio of studies, manage timelines, and ensure CDISC standards and regulatory compliance across submissions.

This senior role requires 8+ years of SAS/Base/Macro/GRAPH programming in biopharma or CRO environments, mentoring junior programmers, and collaborating with cross-functional teams to deliver high-quality results.