Associate Biostatistics Director - Fsp (permanent Home-based)

IQVIA UK

United Kingdom
Fully remote
Phd or ms in biostatistics
8+ years clinical trial statistics experience
Advanced sas and r proficiency
IQVIA UK is seeking an Associate Biostatistics Director for a home-based role responsible for leading biostatistical strategies and methodologies in clinical trials. The ideal candidate should possess extensive experience in clinical trial statistics, advanced technical skills in SAS/R, and a strong background in regulatory submissions

Job Summary

  • The role involves leading the full scope of biostatistics conduct for a specific therapeutic area program within IQVIA UK.
  • Candidates must define statistical strategies, ensure appropriate methodologies for study design, and influence clinical development plans.
  • The position requires representing the team in interactions with major regulatory authorities like the FDA, EMA, and PMDA.

Matching Summary

Match Score: 85

IQVIA UK is seeking an Associate Biostatistics Director for a home-based role responsible for leading biostatistical strategies and methodologies in clinical trials. The ideal candidate should possess extensive experience in clinical trial statistics, advanced technical skills in SAS/R, and a strong background in regulatory submissions.

Skills & Requirements

Must-have

  • PhD or MS in Biostatistics
  • 8+ years clinical trial statistics experience
  • Advanced SAS and R proficiency
  • Strategic study design leadership
  • Regulatory submission experience

Nice-to-have

  • Bayesian methods expertise
  • Predictive modeling skills
  • Simulation techniques knowledge
  • Adaptive design experience
  • FDA/EMA interaction experience

Key Requirements

  • Minimum 8 years experience in clinical trial statistics
  • PhD or MS degree required
  • Experience with Bayesian methods preferred
  • Proven track record in regulatory submissions

Work Rights

Not specified

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