Principal Biostatistician Fsp, Late Phase

IQVIA

Home-based, 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 is seeking a Principal Biostatistician for its Late Phase team, offering a fully remote role to provide statistical support for clinical trials. The ideal candidate should possess a PhD or MS in a relevant field with extensive experience in biostatistics and clinical trials

Job Summary

  • The Principal Biostatistician will provide 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 tables and listings.
  • The role offers home-based remote working opportunities in the U.S. or Canada with a focus on bringing new therapies to market rather than project budgets.

Matching Summary

Match Score: 85

IQVIA is seeking a Principal Biostatistician for its Late Phase team, offering a fully remote role to provide statistical support for clinical trials. The ideal candidate should possess a PhD or MS in a relevant field with extensive experience in biostatistics and clinical trials.

Salary

Base: $115,900.00 - $243,900.00 annualized; Bonus/Equity: Dependent on position offered; Benefits: Range of health and welfare 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
  • Production programming of ADAM and TLF
  • Experience with CDISC SDTM and ADAM standards
  • Proficiency in R or SAS for efficacy/safety analyses

Nice-to-have

  • Interaction with regulators including Advisory Committee meetings
  • 2+ years renal therapeutic or CNS area experience
  • Solid understanding of multiple imputation methods
  • Experience with exploratory analyses
  • Ability to work proactively and independently

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

Cover Letter