At a Glance
- Tasks: Lead statistical analyses for patient-reported outcomes and clinical data.
- Company: Join IQVIA, a leader in healthcare intelligence and clinical research.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Other info: Collaborative global team focused on innovation and diversity.
- Why this job: Make a real impact on patient experiences and drug development.
- Qualifications: Master's or PhD in a quantitative field with 5+ years of experience.
The predicted salary is between 63000 - 77000 £ per year.
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.
Key Responsibilities
- Lead or support statistical analyses for projects involving COA/PRO data.
- Contribute across analysis planning, execution, interpretation, reporting, and client communication.
- 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.
- Contribute to regulatory- and payer-relevant evidence generation.
- Build strong working relationships with clients and cross-functional internal teams.
- Assist in managing the scope of the quantitative analysis workstream.
- 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.
- 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.
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