Global Sap Pp Consultant - Process Excellence

Kion Group Emea; Barcelona; A distancia; EUR 70.000 - 100.000; Jornada completa

Descripción de la vacante

IQVIA in Europe is seeking a Senior Consultant in Statistics and Psychometrics to lead or support analyses of COA/PRO data, on a remote basis. You'll contribute to analysis planning, execution, interpretation, reporting, and client communications to generate scientifically sound, regulatory-relevant evidence for drug development.

Responsibilities include leading workstreams for moderate-complexity projects, developing analysis plans and outputs, applying advanced methods, interpreting results

Formación

• Master's or PhD in biostatistics, statistics, psychometrics, outcomes research, epidemiology, or related quantitative field.
• 5+ years of relevant experience in pharma, biotech, CRO, healthcare, or consulting.
• Advanced knowledge of complex statistical methods for Phase I-IV trials (multivariate, regression, logistic, survival, mixed models).
• Familiarity with SAS and/or R.
• Excellent written and verbal communication skills and ability to work in a matrixed environment.

Responsabilidades

• Lead the quantitative analysis workstream for projects of moderate complexity, ensuring high-quality and timely delivery.
• Develop and review analysis plans, output shells, output specifications, programming requirements, and statistical outputs.
• Apply advanced statistical methods to COA/PRO data and interpret results.
• Communicate methodological choices clearly to internal teams and clients to support decision-making.
• Contribute to regulatory- and payer-relevant evidence generation, including endpoint strategy and scientific communication.
• Build strong client and cross-functional relationships and contribute to proposals and business development.
• Assist in managing the scope, objectives, timelines, and quality of deliverables for the workstream.
• Mentor junior team members and contribute to capability building and process improvements.

Conocimientos

Statistical analyses

COA/PRO data analysis

Communication skills

Regulatory understanding

Educación

Master's/PhD in Biostatistics/Statistics/Psychometrics

Herramientas

SAS

R

Descripción del empleo

Senior Consultant, Statistics and Psychometrics - Remote

Madrid, Spain
Reading, Berkshire, United Kingdom
Amsterdam, Netherlands
London, United Kingdom
Athens, Greece
Full time
R

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

• 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.

This role is not eligible for UK visa sponsorship

EEO Minorities/Females/Protected Veterans/Disabled