Associate Principal, Indirect Treatment Comparison, Evidence Synthesis

IQVIA

Associate Principal overseeing evidence synthesis projects and managing junior staff at IQVIA. Engaging in high-quality deliverables for pharmaceutical clients.

Posted 7/23/2026full-timeRemote • California, New Jersey, North Carolina, Texas • 🇺🇸 United StatesJuniorMid-Level💰 $125,800 - $350,300 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading evidence synthesis projects, including Bayesian Network Meta-Analyses and meta-analysis, while ensuring high-quality deliverables and effective client management. Proficient in project management with strong attention to detail and the ability to communicate effectively across global teams.

Highest-signal resume keywords

PhD In EpidemiologyEvidence Synthesis ResearchBayesian NMAClient Management ExperienceProject Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Meta-AnalysisBayesian Statistical AnalysisSystematic Literature Review (SLR)Data SynthesisProposal DevelopmentContract ManagementQuality CheckingTime ManagementOrganizational Skills

Soft Skills

Attention To DetailProblem SolvingCollaborationEffective Communication

Tools & Technologies

PowerPointExcelWord

Industry Keywords

Pharma ConsultingHealth SciencesRegulatory SubmissionsHTA

About the role

Key responsibilities & impact

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 synthesize data qualitatively and quantitatively, and guide junior staff
Manage projects, oversee the operational, financial, and administrative requirements of projects
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

What you’ll need

PhD in epidemiology or biostatistics (other health sciences okay)
5+ years of experience implementing evidence synthesis research in a pharma consulting environment
Master's in epidemiology or biostatistics (other health sciences okay)
7+ years of experience implementing evidence synthesis research in a pharma consulting environment
Client management experience
5+ years of experience as the client point of contact on projects
Significant and demonstrated experience independently leading projects that included Bayesian NMAs and/or other ITCs
Substantial experience independently leading projects that included meta-analysis, NMA, or other Bayesian statistical analysis
Solid understanding of SLR concepts, guidelines, and required rigor
Strong ability to quality check own and others work so that drafts are delivered with only minimal minor typographical errors
Exceptional attention to detail
Competency in using PowerPoint, Excel, and Word
Fluency in English (spoken and written); strong business/scientific written English
A commitment to working collaboratively and effectively with others in and across the team to accomplish goals
A commitment to timely internal and client communication; with clients, IQVIA project managers and team members, IQVIA colleagues and others
A pragmatic and logical problem solving approach to projects
Strong attention to detail on all project deliverables even under time pressure.
A good understanding of project management with proven time management and personal organizational skills

Benefits

Comp & perks

Health insurance
Retirement plans
Paid time off
Flexible working arrangements
Professional development
Bonuses
Stock options
Equipment allowances
Wellness programs