Lead Evidence Synthesis Principal – ITC/NMA Expert (Remote)

IQVIA

Providence (RI)

Remote

USD 126,000 - 350,000

Full time

14 days+

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Job summary

IQVIA seeks an Associate Principal to lead evidence synthesis projects for pharma clients, guiding junior staff and managing deliverables from start to finish. The role emphasizes ITC, NMAs, and rigorous SLR practices within a global team.

The candidate will drive business development, oversee projects, and coordinate across time zones, ensuring high-quality outputs for HTA and regulatory submissions.

Qualifications

  • Excellent knowledge of systematic literature review (SLR) methods and indirect treatment comparison (ITC).
  • Significant experience leading ITC projects including network meta-analysis and matching adjusted meta-analysis.
  • Global SLR guidelines knowledge and experience implementing them.

Responsibilities

  • Lead implementation of evidence synthesis projects to support HTA and/or regulatory submissions from pre-award to final delivery, and hands on development of deliverables.
  • Lead project teams to ensure the execution of rigorous and high quality deliverables according to timelines.
  • Expert ability to synthesize data qualitatively and quantitatively, and guide junior staff.
  • Project management—manage projects, oversee the operational, financial, and administrative requirements of projects.
  • 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.

Skills

Systematic literature reviews
Indirect treatment comparisons
Bayesian NMAs
Meta-analysis
Project leadership
Client management
Attention to detail
Quality control

Education

Master's in epidemiology or biostatistics
PhD in epidemiology or biostatistics

Tools

PowerPoint
Excel
Word

Job description

IQVIA seeks an Associate Principal to lead evidence synthesis projects for pharma clients, guiding junior staff and managing deliverables from start to finish. The role emphasizes ITC, NMAs, and rigorous SLR practices within a global team.

The candidate will drive business development, oversee projects, and coordinate across time zones, ensuring high-quality outputs for HTA and regulatory submissions.

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