Lead Statistical Programmer: SAS & CDISC Expert

1001 Syneos Health, LLC

North Carolina

Hybrid

USD 81,000 - 145,000

Full time

4 days ago
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Benefits offered by this job

Health benefits
401(k) matching
Stock Purchase Plan
Paid time off
Commissions/Bonus

Job summary

Syneos Health is seeking a Principal Statistical Programmer to join our Sponsor Dedicated team in the US, based in North Carolina. You will lead programming for complex studies, ensure timelines and standards, and mentor junior programmers within a fast-paced biopharma environment.

The role requires 8+ years of SAS/Base/Macro/GRAPH experience, CDISC data standards, and a track record delivering regulatory submissions. We offer competitive compensation and comprehensive benefits.

Qualifications

  • BA/BS degree (MS preferred) in statistics or computer science.
  • 8+ years of programming experience using SAS in biopharma/CRO.
  • Experience with CDISC standards and electronic submissions.
  • Strong organizational and leadership skills; able to mentor juniors.

Responsibilities

  • Function as a Lead programmer for a compound or group of studies.
  • Maintain overall timeline and programming standards.
  • Review standard macros and datasets used.
  • Mentor junior programmers on internal systems and standards.
  • Assist junior programmers in new study setup.
  • Review production area after study programming is complete.
  • Check validation reports are clean and properly documented.
  • Review CDISC validation output.
  • Act as Programming lead for a submission project.
  • Serve as expert to provide solutions to complex problems.

Skills

SAS/Base/Macro/GRAPH
Lead programmer

Education

BA/BS in Statistics or Computer Science

Tools

SAS
CDISC

Job description

Syneos Health is seeking a Principal Statistical Programmer to join our Sponsor Dedicated team in the US, based in North Carolina. You will lead programming for complex studies, ensure timelines and standards, and mentor junior programmers within a fast-paced biopharma environment.

The role requires 8+ years of SAS/Base/Macro/GRAPH experience, CDISC data standards, and a track record delivering regulatory submissions. We offer competitive compensation and comprehensive benefits.

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