Conseiller(ère) Principal(e) Et Statisticien(ne), Recherche Centrée Sur Le Patient -- Senior Consultant And Statistician, Patient Centered Research

IQVIA UK

Base: $114,100.00 - $164,100.00 annualized; bonus/...
Not specified
Advanced statistical methods for clinical trials
Sas or r programming proficiency
Experience with coa and pro data analysis
IQVIA UK is seeking a Senior Consultant and Statistician for their Patient-Centered Research team. The role involves leading statistical analyses and providing evidence that informs clinical development and regulatory strategies while mentoring junior team members

Job Summary

  • This role leads quantitative analysis workstreams for projects involving Clinical Outcome Assessments (COA) and Patient-Reported Outcomes (PRO).
  • The position requires applying advanced statistical methods to Phase I-IV clinical trial data to generate evidence for regulatory and payer decisions.
  • Candidates will mentor junior staff, contribute to business development activities, and collaborate within a global team focused on patient-centered research.

Matching Summary

Match Score: 85

IQVIA UK is seeking a Senior Consultant and Statistician for their Patient-Centered Research team. The role involves leading statistical analyses and providing evidence that informs clinical development and regulatory strategies while mentoring junior team members.

Salary

Base: $114,100.00 - $164,100.00 annualized; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Health, wellness, and other benefits included

Skills & Requirements

Must-have

  • Advanced statistical methods for clinical trials
  • SAS or R programming proficiency
  • Experience with COA and PRO data analysis
  • PhD or Master's in biostatistics or related field
  • 5+ years pharmaceutical industry experience

Nice-to-have

  • Strong client communication skills
  • Mentoring junior team members
  • Business development and proposal support
  • Knowledge of regulatory submission strategies

Key Requirements

  • Master's degree or PhD in Biostatistics, Statistics, Psychometrics, Epidemiology
  • Minimum 5 years of relevant experience in pharma, biotech, CRO, or consulting
  • Proficiency in SAS and/or R for statistical programming

Work Rights

Not specified

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