Associate Principal, Indirect Treatment Comparison (ITC), Evidence Synthesis

Durham, NC · Austin, TX · New Providence, NJ · San Francisco, CA · Carlsbad, CA · New York, NY · Northborough, MA · Rockville, MD · Chesapeake, VA · Milwaukee, WI · Richmond, VA · Boston, MA · Providence, RI · Rosemont, IL · San Mateo, CA · Greenwich, CT · Bethlehem, PA · Falls Church, VA · Marietta, GA · Parsippany, NJ · Wayne, PAFull-time$126k–$350kPosted Jul 23, 2026

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Location: Remote, must be based in US

OVERVIEW

Associate Principals are methodologic experts with substantial experience in providing consulting services to Pharmaceutical clients. Associate Principals are project leaders who are responsible for implementing rigorous evidence synthesis research, overseeing the work of junior staff, and proactively managing the project timeline. They are detail oriented, act on anticipated project needs, and problem solve. Associate Principals contribute to the operational and fiscal health of the overall practice and training/success of junior staff.

REQUIRED KNOWLEDGE

Excellent knowledge of systematic literature review (SLR) methods and indirect treatment comparison (ITC). Significant experience leading and conducting ITC projects, including network meta-analysis, matching adjusted meta-analysis, etc. Expert understanding of global SLR guidelines and best practices, and substantial experience in implementing them.

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

QUALIFICATIONS, EXPERIENCE, TECHNICAL AND PERSONAL SKILLS

Experience

Preferred:

PhD in epidemiology or biostatistics (other health sciences okay)
5+ years of experience implementing evidence synthesis research in a pharma consulting environment

Minimum required:

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

Must have 5+ years of experience as the client point of contact on projects

Technical skills and knowledge

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

Essential personal skills and behaviors

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

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $125,800.00 - $350,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.