The Patient Reported Outcomes Manager reports to a Clinical Program Development (CPD) Program Lead and will be responsible for ensuring timely, adequate, cost effective business aligned standards ...
The Patient Reported Outcomes Manager reports to a Clinical Program Development (CPD) Program Lead and will be responsible for ensuring timely, adequate, cost effective business aligned standards ...
Director, Psychometrics & Patient-Reported Outcomes (PRO) Strategy Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on ...
Director, Psychometrics & Patient-Reported Outcomes (PRO) Strategy Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on ...
$23.06 - $32.29/hr
Supports research projects focused on the development, validation, and analysis of patient-reported (PRO) outcome measures in academic research and Contract Research Organization environments.
$23.06 - $32.29/hr
Supports research projects focused on the development, validation, and analysis of patient-reported (PRO) outcome measures in academic research and Contract Research Organization environments.
$23.06 - $32.29/hr
Supports research projects focused on the development, validation, and analysis of patient-reported (PRO) outcome measures in academic research and Contract Research Organization environments.
$23.06 - $32.29/hr
Supports research projects focused on the development, validation, and analysis of patient-reported (PRO) outcome measures in academic research and Contract Research Organization environments.
Ensure that patient reported outcome tools selected for clinical development programs are appropriate to the indication, scientifically valid, and acceptable to health authorities. Develop and ...
Ensure that patient reported outcome tools selected for clinical development programs are appropriate to the indication, scientifically valid, and acceptable to health authorities. Develop and ...
Patient reported outcomes: Lead the integration of patient voice through quality-of-life instruments into clinical trials and oversee the design of patient surveys and validated instruments for ...
Patient reported outcomes: Lead the integration of patient voice through quality-of-life instruments into clinical trials and oversee the design of patient surveys and validated instruments for ...
Provide guidance on FDA regulations related to patient-reported outcomes (PROs) and patient-focused drug development (PFDD), ensuring alignment with labeling claims * Prepare regulatory-grade ...
Provide guidance on FDA regulations related to patient-reported outcomes (PROs) and patient-focused drug development (PFDD), ensuring alignment with labeling claims * Prepare regulatory-grade ...
Director, Health Economics & Outcomes Research (HEOR)
Berkeley Heights, NJ · On-site
$168K - $268K/yr
Provide guidance on FDA regulations related to patient-reported outcomes (PROs) and patient-focused drug development (PFDD), ensuring alignment with labeling claims * Prepare regulatory-grade ...
Director, Health Economics & Outcomes Research (HEOR)
Berkeley Heights, NJ · On-site
$168K - $268K/yr
Provide guidance on FDA regulations related to patient-reported outcomes (PROs) and patient-focused drug development (PFDD), ensuring alignment with labeling claims * Prepare regulatory-grade ...
Provide guidance on FDA regulations related to patient-reported outcomes (PROs) and patient-focused drug development (PFDD), ensuring alignment with labeling claims * Prepare regulatory-grade ...
Provide guidance on FDA regulations related to patient-reported outcomes (PROs) and patient-focused drug development (PFDD), ensuring alignment with labeling claims * Prepare regulatory-grade ...
Provide guidance on FDA regulations related to patient-reported outcomes (PROs) and patient-focused drug development (PFDD), ensuring alignment with labeling claims * Prepare regulatory-grade ...
Provide guidance on FDA regulations related to patient-reported outcomes (PROs) and patient-focused drug development (PFDD), ensuring alignment with labeling claims * Prepare regulatory-grade ...
Provide guidance on FDA regulations related to patient-reported outcomes (PROs) and patient-focused drug development (PFDD), ensuring alignment with labeling claims * Prepare regulatory-grade ...
Provide guidance on FDA regulations related to patient-reported outcomes (PROs) and patient-focused drug development (PFDD), ensuring alignment with labeling claims * Prepare regulatory-grade ...
Responsible for including patient-reported outcomes studies into NDA/MAA dossiers and labels, and interacting with Agencies. Report, publish and disseminate HEOR data and study results in compliance ...
Responsible for including patient-reported outcomes studies into NDA/MAA dossiers and labels, and interacting with Agencies. Report, publish and disseminate HEOR data and study results in compliance ...
Senior RWE Statistical Programmer (PRO) - FSP
Durham, NC · On-site
$88K - $220K/yr
The role includes integrating patient-reported outcomes (PRO) with clinical endpoints, linking survey and real-world data to generate actionable insights, and ensuring the quality of survey and ...
Senior RWE Statistical Programmer (PRO) - FSP
Durham, NC · On-site
$88K - $220K/yr
The role includes integrating patient-reported outcomes (PRO) with clinical endpoints, linking survey and real-world data to generate actionable insights, and ensuring the quality of survey and ...
... of Patient Reported Outcomes (PRO) strategies ensuring PRO end points in product labeling and support product differentiation. • Develop and validate PRO endpoints for integration in pivotal ...
... of Patient Reported Outcomes (PRO) strategies ensuring PRO end points in product labeling and support product differentiation. • Develop and validate PRO endpoints for integration in pivotal ...
Senior RWE Statistical Programmer (PRO) - FSP
Durham, NC · On-site
$88K - $220K/yr
The role includes integrating patient-reported outcomes (PRO) with clinical endpoints, linking survey and real-world data to generate actionable insights, and ensuring the quality of survey and ...
Senior RWE Statistical Programmer (PRO) - FSP
Durham, NC · On-site
$88K - $220K/yr
The role includes integrating patient-reported outcomes (PRO) with clinical endpoints, linking survey and real-world data to generate actionable insights, and ensuring the quality of survey and ...
Sr. Director, Global Head of Health Economics & Outcomes Research (Hybrid-Acton, MA or San Diego,...
Reporting to the VP of Global HEMA, the incumbent will lead a global team of experts in HEOR and real-world evidence (RWE) study design, epidemiology, biostatistics, patient-reported outcomes (PROs ...
New
Sr. Director, Global Head of Health Economics & Outcomes Research (Hybrid-Acton, MA or San Diego,...
Reporting to the VP of Global HEMA, the incumbent will lead a global team of experts in HEOR and real-world evidence (RWE) study design, epidemiology, biostatistics, patient-reported outcomes (PROs ...
New
... and patient- reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP ...
... and patient- reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP ...
Director, Outcomes Research
Rahway, NJ · On-site
... and patient- reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP ...
Director, Outcomes Research
Rahway, NJ · On-site
... and patient- reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP ...
... and patient- reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP ...
... and patient- reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP ...
Sr. Director, Global Head of Health Economics & Outcomes Research (Hybrid-Acton, MA or San Diego,...
Reporting to the VP of Global HEMA, the incumbent will lead a global team of experts in HEOR and real-world evidence (RWE) study design, epidemiology, biostatistics, patient-reported outcomes (PROs ...
New
Sr. Director, Global Head of Health Economics & Outcomes Research (Hybrid-Acton, MA or San Diego,...
Reporting to the VP of Global HEMA, the incumbent will lead a global team of experts in HEOR and real-world evidence (RWE) study design, epidemiology, biostatistics, patient-reported outcomes (PROs ...
New
Patient Reported Outcomes information
See salary details
$11.54 - $12.37
3% of jobs
$12.37 - $13.20
4% of jobs
$13.20 - $14.03
3% of jobs
$14.03 - $14.86
7% of jobs
$15.16 is the 25th percentile. Wages below this are outliers.
$14.86 - $15.69
20% of jobs
The median wage is $16.29 / hr.
$15.69 - $16.52
17% of jobs
$16.52 - $17.35
20% of jobs
$17.37 is the 75th percentile. Wages above this are outliers.
$17.35 - $18.18
11% of jobs
$18.18 - $19.01
5% of jobs
$19.01 - $19.84
2% of jobs
$19.84 - $20.67
7% of jobs
$11
$16
$20
How much do patient reported outcomes jobs pay per hour?
What are the key skills and qualifications needed to thrive as a Patient Reported Outcomes (PRO) Specialist, and why are they important?
What is the difference between Patient Reported Outcomes vs Clinical Data Analysts?
| Aspect | Patient Reported Outcomes | Clinical Data Analysts |
|---|---|---|
| Credentials | Typically require healthcare or research background, often with degrees in health sciences or related fields | Require strong statistical, analytical, and data management skills, often with degrees in statistics, data science, or related fields |
| Work Environment | Healthcare settings, research institutions, or clinical trial environments | Hospitals, research organizations, pharmaceutical companies, or healthcare analytics firms |
| Employer & Industry Usage | Used to gather patient perspectives on health status and treatment outcomes | Analyze clinical data to support research, regulatory submissions, and healthcare decision-making |
While Patient Reported Outcomes focus on collecting patient perspectives on health and treatment effects, Clinical Data Analysts interpret and analyze clinical data to support research and healthcare decisions. Both roles are vital in healthcare but serve different functions in improving patient care and advancing medical research.
How does a professional working in Patient Reported Outcomes typically collaborate with clinical and research teams?
What are Patient Reported Outcomes?
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Full-time
Medical, Dental, Vision, Retirement, PTO
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AbbVie rating
8.7
Based on 97 frontline employees who took The Breakroom Quiz
13th of 73 rated pharmaceutical
Job description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
The Patient Reported Outcomes Manager reports to a Clinical Program Development (CPD) Program Lead and will be responsible for ensuring timely, adequate, cost effective business aligned standards, strategies and processes related to Patient Report Outcomes on behalf of the Clinical Development organization.
Responsibilities
- Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
Provide project management and expert consultation supporting patient centered/PRO licensing and translation activities for all Therapeutic Areas within Clinical Program Development (CPD). - Serve as the owner of the Vault PRO Library which is a repository for PROs and includes licensing and permission details & terms; MSAs with AbbVie; translation requirements; training requirements; electronic format requirements; etc.
- Interact with PRO owners, Outsourcing, HEOR, Data Sciences and the clinical teams to drive and facilitate the PRO and ePRO implementation with respect to vendor contract initiation, translation management, project milestones, timelines, and deliverables during Study Start up.
- Provide strategic & technical expertise and training to the CPD organization in support of PRO/ePRO activities during study start up.
Provides direct supervision to PRO management associate(s) creating an inclusive and innovative environment
- Bachelor's Degree in a scientific field or equivalent with relevant experience is acceptable
A minimum of 6 years of global (direct or peripheral) clinical research or project management experience.
Must have knowledge and minimum 2 year hands on and relevant experience with Patient Reported Outcomes or outcomes research. - Demonstrates a high level of core and technical competencies through management of various components of the PRO/ePRO process.
Possesses good communication skills and demonstrated leadership abilities
Competent in application of standard business procedures (Standard Operating Procedures) and understand the global environment from an operations and regulatory/ (GCP) Good Clinical Practices) perspective. - Must have experience building effective working relationships across functions and geographic locations.
- Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance
Learns, fast, grasps the 'essence' and can change the course quickly where indicated
Raises the bar and is never satisfied with the status quo
Creates a learning environment, open to suggestions and experimentation for improvement
Embraces the ideas of others, nurtures innovation and manages innovation to reality
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our long-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
About AbbVie
Sourced by ZipRecruiter
AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
North Chicago, IL, US
Year founded
2013