Lead Evidence Synthesis & ITC Expert (Remote)

IQVIA

Northborough (MA)

On-site

USD 126,000 - 350,000

Full time

13 days ago
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Job summary

IQVIA is seeking an Associate Principal to lead evidence synthesis projects for pharmaceutical clients, with responsibility from pre-award to final delivery. You will manage teams, guide junior staff, and ensure rigorous deliverables across time zones in a remote US-based setting.

Requires 7+ years in pharma consulting evidence synthesis, including ITCs and NMAs, plus strong client contact experience. Proficiency in PowerPoint, Excel and Word is expected; English fluency is essential.

Qualifications

  • PhD in epidemiology or biostatistics (other health sciences okay).
  • 7+ years of experience implementing evidence synthesis research in a pharma consulting environment.
  • Master's in epidemiology or biostatistics (other health sciences okay).
  • Must have 5+ years of experience as the client point of contact on projects.

Responsibilities

  • Lead implementation of evidence synthesis projects to support HTA and/or regulatory submissions from pre-award to final delivery, as well as 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

Bayesian NMAs
ITCs
English fluency
Project management
Data synthesis
PPT
Excel
Word

Education

PhD in epidemiology/biostatistics
Master's in epidemiology/biostatistics

Tools

PowerPoint
Excel
Word

Job description

IQVIA is seeking an Associate Principal to lead evidence synthesis projects for pharmaceutical clients, with responsibility from pre-award to final delivery. You will manage teams, guide junior staff, and ensure rigorous deliverables across time zones in a remote US-based setting.

Requires 7+ years in pharma consulting evidence synthesis, including ITCs and NMAs, plus strong client contact experience. Proficiency in PowerPoint, Excel and Word is expected; English fluency is essential.

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