Remote Associate Principal, Evidence Synthesis & ITC

IQVIA

San Mateo (CA)

On-site

USD 140,000 - 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 in a remote US-based role. You will oversee project teams, deliver rigorous ITC and NMA analyses, and guide junior staff across time zones.

You will drive proposals, participate in business development, ensure timely delivery, and uphold high standards of methodological rigor for HTA and regulatory submissions.

Qualifications

  • Expert knowledge of SLR methods and ITC; significant ITC project leadership experience.
  • Experience with network meta-analysis and matching-adjusted indirect comparisons.
  • Strong understanding of global SLR guidelines and best practices.

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
Network meta-analysis
Indirect treatment comparisons
Evidence synthesis
Project leadership
Client management

Education

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

Tools

PowerPoint
Excel
Word

Job description

IQVIA is seeking an Associate Principal to lead evidence synthesis projects for pharmaceutical clients in a remote US-based role. You will oversee project teams, deliver rigorous ITC and NMA analyses, and guide junior staff across time zones.

You will drive proposals, participate in business development, ensure timely delivery, and uphold high standards of methodological rigor for HTA and regulatory submissions.

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