Senior Consultant and Statistician, Patient-Centered Research
Overview
At IQVIA, the Patient Centered Solutions team helps clients generate robust evidence on the patient experience across clinical development, regulatory submissions, and scientific dissemination. Our Statistics & Psychometrics team specializes in the analysis of clinical outcome assessment (COA) and patient-reported outcomes (PRO) data, combining scientific rigor with strategic consulting to support high-impact decisions in drug development.
The Role
As a Senior Consultant, you will lead or support statistical analyses for projects involving COA/PRO data. You will contribute across analysis planning, execution, interpretation, reporting, and client communication, helping deliver evidence that is scientifically sound, regulatory-relevant, and clearly communicated.
Key Responsibilities
- Lead the quantitative analysis workstream for projects of moderate complexity, ensuring high-quality, timely, and scientifically sound delivery.
- Develop and review analysis plans, output shells, output specifications, programming requirements, statistical outputs, and technical reports.
- Apply advanced statistical methods to COA/PRO data.
- Interpret results clearly and credibly for internal teams and clients and communicate methodological choices in a way that supports decision-making.
- Contribute to regulatory- and payer-relevant evidence generation, including support for endpoint strategy and scientific communication.
- Build strong working relationships with clients and cross-functional internal teams, and contribute to proposals, bid defenses, and business development activities.
- Assist in managing scope of the quantitative analysis workstream, including objectives, timelines and quality of deliverables.
- Mentor junior team members and contribute to team capability building, training, standards, and process improvement.
Qualifications
- Master’s degree or PhD in biostatistics, statistics, psychometrics, outcomes research, epidemiology, or a related quantitative field.
- 5+ years of relevant experience in the pharmaceutical, biotech, CRO, healthcare, or consulting environment.
- Advanced knowledge of complex statistical methods that apply to Phase I-IV clinical trials (multivariate analysis, regression analysis, logistic analysis, survival analysis, mixed models repeated measures, etc.).
- Familiarity with SAS and/or R.
- Excellent written and verbal communication skills, strong attention to detail, and the ability to work effectively in a collaborative, matrixed environment.
Why Join Us
This role offers the opportunity to work on specialized, patient-centered research that informs clinical development, regulatory strategy, and evidence communication across a wide range of therapeutic areas. You will join a collaborative global team with deep expertise in COA analysis, psychometrics, and advanced statistical methodology.
This role is not eligible for UK visa sponsorship
EEO Minorities/Females/Protected Veterans/Disabled
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