Senior Consultant and Statistician (Patient Centered Research) mwd

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.
• Assists in managing the 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

• Masters 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

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

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.