Remote Principal Statistical Programmer & Lead Mentor

Syneos Health, Inc.; Massachusetts; Hybrid; USD 81,000 - 145,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (Medical, Dental, Vis­

401k match

Employee Stock Purchase Plan

Bonus / commissions

Paid time off and sick time

Job summary

Syneos Health is seeking a Principal Statistical Programmer Sponsor Dedicated for US hiring. The role emphasizes senior-level SAS programming expertise, CDISC data standards, and leadership of junior programmers on sponsor-driven studies.

The position offers a remote-friendly setup with a strong emphasis on timely delivery, high-quality programming, and regulatory-compliant submissions across biopharmaceutical programs.

Qualifications

• Minimum 8 years of programming experience using SAS/Base/Macro/GRAPH in biopharma or CRO industries.
• Data Management experience including CDISC standard is highly desirable.
• Strong SAS programming skills and attention to detail.

Responsibilities

• Maintain the overall timeline for studies.
• Maintain programming standards for studies.
• Review macros and datasets used.
• Discuss resource needs for the group of studies.
• Mentor junior programmers on Incyte systems and standards.
• Assist junior programmers in new study setup.
• Ensure datasets, programs, and outputs are properly stored and documented.
• Review CDISC validation outputs and ensure clean validation summaries.
• Lead programming for submissions under supervision.
• Mentor and provide expert recommendations on complex problems.

Skills

SAS programming

Mentoring juniors

Regulatory knowledge

Education

BS degree in statistics or computer science

Tools

SAS/Base/Macro/GRAPH

Job description

Syneos Health is seeking a Principal Statistical Programmer Sponsor Dedicated for US hiring. The role emphasizes senior-level SAS programming expertise, CDISC data standards, and leadership of junior programmers on sponsor-driven studies.

The position offers a remote-friendly setup with a strong emphasis on timely delivery, high-quality programming, and regulatory-compliant submissions across biopharmaceutical programs.