Description
We are seeking a Consultant Principal, Statistician to join our team. As an Associate Principal, you will be a methodological expert with substantial experience in providing consulting services to pharmaceutical clients. You will lead the implementation of evidence synthesis research, oversee the work of junior staff, and proactively manage project timelines.
Responsibilities:
- Lead implementation of evidence synthesis projects to support HTA and/or regulatory submissions from pre-award to final delivery
- Lead project teams to ensure the execution of rigorous and high-quality deliverables according to timelines
- Expert ability to synthesise data qualitatively and quantitatively, and guide junior staff
- Project management – manage projects, oversee operational, financial, and administrative requirements
- Business development – independently qualify leads, develop proposals, attend bid defenses, and manage the contracting process
- Support more senior staff on specific business initiatives as required
- Work effectively across time zones as part of a global team
Requirements:
- Master's degree in Epidemiology, Pharmacology, Public Health, or Biostatistics (or related field)
- 7+ years of experience leading evidence synthesis research projects
- Excellent knowledge of systematic literature review (SLR) methods and indirect treatment comparison (ITC)
- Significant experience leading and conducting ITC projects, including network meta-analysis and matching adjusted meta-analysis
- Strong understanding of SLR concepts, guidelines, and required rigor
- Exceptional attention to detail and ability to quality check own and others' work
- Fluency in English (spoken and written)
Nice to Have:
- PhD in Epidemiology, Public Health, or Biostatistics (or related field)
- 5+ years of experience leading evidence synthesis research projects
- Experience with Bayesian NMAs and/or other ITCs
What We Offer:
- Competitive salary
- Opportunity to work with a global team
- Collaborative and dynamic work environment