IQVIA UK is seeking a Principal Biostatistician for Early Phase Clinical Development, with a focus on drug development programs involving pharmacokinetics (PK) and pharmacodynamics (PD). This fully remote position offers the opportunity to work with leading pharmaceutical and biotech companies while providing statistical support for clinical trials
Job Summary
The Principal Biostatistician is responsible for providing statistical support for drug development programs in early phases, focusing on healthy normal studies with PK and PD endpoints.
Candidates will write statistical sections of clinical trial protocols, review eCRFs, and provide guidance to programmers in authoring analysis dataset specifications.
This role offers home-based remote working opportunities within the U.S. or Canada, along with a focus on work-life balance and long-term job stability.
Matching Summary
Match Score: 85
IQVIA UK is seeking a Principal Biostatistician for Early Phase Clinical Development, with a focus on drug development programs involving pharmacokinetics (PK) and pharmacodynamics (PD). This fully remote position offers the opportunity to work with leading pharmaceutical and biotech companies while providing statistical support for clinical trials.
Salary
Base: $126,800.00 - $235,400.00 annualized; Bonus/Equity: Not specified; Benefits: Health, wellness, and other benefits available
Skills & Requirements
Must-have
PhD or MS in Statistics/Biostatistics
3+ years pharmaceutical industry experience
2+ years non-compartmental PK analysis
Proficiency in SAS and/or R programming
Experience with CDISC standards (SDTM, ADaM)
Knowledge of ICH GCP and regulatory guidance
Nice-to-have
Experience with statistical modeling and simulations
Background in pharmacodynamic/biomarker analyses
Ability to supervise programmers constructively
Strong project management and decision-making skills
Key Requirements
Doctorate or Master's degree in Statistics or related field
Minimum 3 years industry experience (PhD) or 5 years (MS)
Valid work authorization for US or Canada required
Work Rights
Must have valid work authorization for US or Canada