Data Analyst, PRO/COA Psychometrics

Lensa; Durham (NC); Remote; USD 106,000 - 177,000; Part time

Job summary

Lensa is seeking a Data Analyst for the Real-World Solutions team at IQVIA, focusing on PRO/COA psychometrics. The role entails managing analyses for health-related observational and clinical trial data, requiring expertise in statistical programming and observational research. Candidates with a Master's or PhD in a related field are encouraged to apply for this dynamic opportunity that supports data analysis critical to patient outcomes.

Qualifications

• 2 years of relevant experience or 1-year experience with PhD.
• Knowledge of PRO/COA methodologies.
• Strong written and verbal communication skills.

Responsibilities

• Develop statistical analysis plans.
• Conduct QC programming for studies using clinical trial data.
• Communicate timelines and results to the project team.

Skills

Statistical programming

Observational research

Clinical trial data analysis

Psychometric analysis

Education

Master’s degree in psychometrics, statistics, or related field

PhD in psychometrics

Tools

SAS

R

M-Plus

Job description

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Data Analyst – PRO/COA Psychometrics

Location : home-based anywhere in the United States only

Job Overview

IQVIA is hiring to expand our FSP team, working fully within the environment of a prominent pharmaceutical company. The Data Analyst role is part of our Real-World Solutions team and is responsible for leading analyses related to PRO/COA endpoints using health-related observational and clinical trial data under one client portfolio. This individual must have expertise in observational research and clinical trial data analysis, strong statistical programming skills, and experience managing multiple studies and complex analyses. Psychometric analysis experience is a plus.

Essential Functions

• Develop statistical analysis plans for descriptive and complex statistics in studies using clinical trial data for PRO/COA endpoint research questions
• Support integration of PRO clinical trial results into value dossiers and regulatory submission packages
• Lead development of statistical programs for regulatory and non-regulatory submissions (pre-defined and post-hoc)
• Understand CDISC-structured data as required for project deliverables
• Conduct QC programming for descriptive and complex studies using clinical trial data
• Contribute to writing study reports and utilize visualization tools for reporting and data synthesis
• Communicate timelines, progress reports, and results to the project team and key stakeholders
• Provide technical, programming, and statistical expertise, and independently deliver project solutions for complex studies
• Collaborate closely with the scientific team to develop and refine analytic procedures and workflows
  
  

Qualifications

• Master’s degree in psychometrics, statistics, biostatistics, measurement science, analytic psychology, or a related field with 2 years of relevant experience, or a PhD in psychometrics with 1 year of relevant experience. Relevant years of experience will be considered in lieu of a degree
• Knowledge of PRO/COA methodologies, statistics, and programming required
• Demonstrated proficiency in statistical programming using SAS, R, or M-Plus
• Strong knowledge and experience conducting PRO endpoint psychometric analyses using clinical trial data required
• Significant experience in the psychometric evaluation of outcome measures, including classical psychometric methods, exploratory and confirmatory factor analysis, and/or Item Response Theory
• Strong written and verbal communication skills, including technical writing
• Ability to effectively manage and prioritize multiple tasks and projects
  
  

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

The potential base pay range for this role, when annualized, is $106,200.00 - $177,000.00. 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled

If you have questions about this posting, please contact [e-mail]

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Part-time

Job function

• Job function

  Information Technology

• Industries

  IT Services and IT Consulting

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