Principal Statistical Lead, Clinical Trials

BioSpace

Boston (MA)

Presencial

USD 194 000 - 308 000

Tempo integral

há 10 horas
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Vantagens oferecidas por esta oferta de emprego

401(k) matching
Pension plan
Vacation benefits
Medical, dental, vision
Flexible benefits
Life insurance

Resumo da oferta

Lilly seeks a seasoned Statistician/Biostatistician to lead clinical trial design, analysis, and interpretation at the program level. You will influence decisions with robust statistical methods and collaborate across functions to ensure data quality and regulatory readiness.

Responsibilities include protocol input, SAP creation, and communicating results for submissions and publications. Strong SAS/R/Spotfire skills and DMC and regulatory experience are required.

Qualificações

  • Ph.D. in Statistics or Biostatistics.
  • 7+ years of experience in clinical research and development in the pharmaceutical industry.
  • Experience with data monitoring committees (DMC) and regulatory submissions.

Responsabilidades

  • Lead development of clinical plans, innovative study designs, and interpretation of results at the program level.
  • Select statistical methods, write SAP sections, and conduct analyses.
  • Collaborate with data sciences to ensure data quality and methodological rigor.
  • Communicate study results via regulatory submissions, manuscripts, or presentations.

Conhecimentos

statistical leadership
teamwork
communication
regulatory collaboration
statistical programming

Formação académica

Ph.D. in Statistics or Biostatistics

Ferramentas

SAS
R
Spotfire

Descrição da oferta de emprego

Lilly seeks a seasoned Statistician/Biostatistician to lead clinical trial design, analysis, and interpretation at the program level. You will influence decisions with robust statistical methods and collaborate across functions to ensure data quality and regulatory readiness.

Responsibilities include protocol input, SAP creation, and communicating results for submissions and publications. Strong SAS/R/Spotfire skills and DMC and regulatory experience are required.

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