Senior Epidemiological Programming Lead (SAS/R)

Cytel

Richmond (VA)

On-site

USD 140,000 - 210,000

Full time

14 days+
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Job summary

Cytel is seeking an Associate Director, Epidemiological Statistical Programming to lead and mentor a team of statisticians and programmers. You will translate study objectives into robust SAS and/or R solutions for epidemiological and real-world evidence studies, ensuring high quality, reproducible analyses.

You will collaborate with cross-functional teams, oversee complex programming tasks, and drive standardization and automation to support diverse therapeutic areas.

Qualifications

  • Strong programming in SAS and/or R required.
  • 8+ years in statistical programming within pharma/biotech/Life Sciences.
  • Experience with epidemiology, RWE, HEOR studies.
  • Leadership and mentoring of programmers across projects.

Responsibilities

  • Provide technical leadership to epidemiological programmers.
  • Lead analysis for epidemiological and RWE studies.
  • Develop and maintain SAS/R programs for analyses and outputs.
  • Collaborate with epidemiologists, statisticians, and data scientists.
  • Review deliverables for accuracy and timelines.
  • Support data sources including administrative claims and EHR.
  • Develop programming standards and reusable tools.
  • Mentor junior staff and promote best practices.

Skills

Technical leadership
Mentorship
SAS programming
R programming
Epidemiology programming
Observational/RWE studies
Cross-functional collaboration
Regulatory/QA
Project prioritization
Data quality control
Team leadership

Education

Bachelor's degree in Statistics/Biostatistics/Epidemiology/Data Science

Tools

SAS
R
Data sources: claims, EHR, registries

Job description

Cytel is seeking an Associate Director, Epidemiological Statistical Programming to lead and mentor a team of statisticians and programmers. You will translate study objectives into robust SAS and/or R solutions for epidemiological and real-world evidence studies, ensuring high quality, reproducible analyses.

You will collaborate with cross-functional teams, oversee complex programming tasks, and drive standardization and automation to support diverse therapeutic areas.

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