Principal Biostatistician Fsp, Late Phase

IQVIA UK

United States
Base: $115,900.00 - $243,900.00 annualized; bonus/...
Fully remote
Phd or ms in statistics/biostatistics
5+ years industry experience required
3+ years phase 2/3 clinical trial experience
IQVIA UK is seeking a Principal Biostatistician for its Late Phase team, offering a fully remote position within a global CRO that partners with leading pharmaceutical and biotech companies. The role focuses on providing statistical support for clinical trials and requires extensive experience in biostatistics, particularly in Phase 2/3 clinical trials

Job Summary

  • The Principal Biostatistician provides statistical support for pharmaceutical clinical trials in patients within a Functional Service Provider partnership.
  • Responsibilities include authoring statistical analysis plans, production programming of efficacy datasets, and supervising programmers for safety analyses.
  • The role offers home-based remote working opportunities with a focus on bringing new therapies to market rather than project budgets.

Matching Summary

Match Score: 85

IQVIA UK is seeking a Principal Biostatistician for its Late Phase team, offering a fully remote position within a global CRO that partners with leading pharmaceutical and biotech companies. The role focuses on providing statistical support for clinical trials and requires extensive experience in biostatistics, particularly in Phase 2/3 clinical trials.

Salary

Base: $115,900.00 - $243,900.00 annualized; Bonus/Equity: Incentive plans may be offered; Benefits: Health, welfare, and other benefits included

Skills & Requirements

Must-have

  • PhD or MS in Statistics/Biostatistics
  • 5+ years industry experience required
  • 3+ years Phase 2/3 clinical trial experience
  • Proficiency in R or SAS programming
  • Experience with CDISC standards (SDTM, ADAM)
  • Production programming of efficacy datasets

Nice-to-have

  • Interaction with regulators and Advisory Committees
  • Renal therapeutic or CNS area experience
  • Multiple imputation methods expertise
  • Collaboration with cross-functional sponsor teams

Key Requirements

  • PhD in Statistics with 5+ years experience
  • MS in Statistics with 7+ years experience
  • At least 3 years in Phase 2/3 clinical trials
  • Understanding of ICH GCP and ICH E9 guidelines

Work Rights

Not specified

Tailored Resume

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