Senior Lead Biostatistician – Oncology Evidence Gen

Labcorp

Durham (NC)

On-site

USD 120,000 - 180,000

Full time

13 days ago

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Benefits offered by this job

Medical, Dental, Vision
401(k) and Stock Purchase Plan
Paid Time Off

Job summary

Labcorp in Raleigh/Durham, NC, seeks a Senior Lead Biostatistician to lead statistical strategy for oncology evidence generation, MRD-focused studies, observational research, registries and real-world data. You will serve as the central statistical leader across studies, ensuring proper design, power, and rigorous analyses.

You will partner with clinical development, science, data and external collaborators to translate complex data into meaningful insights that support publication and clinical

Qualifications

  • MS in Biostatistics or related quantitative field.
  • 6+ years of experience in clinical biostatistics.
  • 5+ years of statistical programming (R, SAS).
  • 3+ years experience supporting clinical studies (observational/registries).
  • 3+ years independently managing analyses across multiple studies.

Responsibilities

  • Design MRD-focused studies, define endpoints and analysis strategy.
  • Perform sample size and power calculations; draft SAPs.
  • Conduct statistical analyses across diverse data (clinical, registries, real-world).
  • Serve as statistical lead; communicate methods/results to non-statistical stakeholders.
  • Identify risks and provide data-driven recommendations.
  • Develop statistical deliverables and study reports; contribute to publications.
  • Lead or contribute to templates, tools, and workflows; build MRD/oncology expertise.

Skills

Clinical biostatistics
Statistical programming (R, SAS)
Study design & analysis
Leadership & project management

Education

MS in Biostatistics, Statistics, or related field
PhD in Biostatistics, Statistics, or related field

Tools

R
SAS

Job description

Labcorp in Raleigh/Durham, NC, seeks a Senior Lead Biostatistician to lead statistical strategy for oncology evidence generation, MRD-focused studies, observational research, registries and real-world data. You will serve as the central statistical leader across studies, ensuring proper design, power, and rigorous analyses.

You will partner with clinical development, science, data and external collaborators to translate complex data into meaningful insights that support publication and clinical

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