Lead the development, adaptation, and evaluation of clinical outcome assessments (COAs), including patient-reported outcomes (PROs), observer-reported outcomes (ObsROs), clinician-reported outcomes ...
Lead the development, adaptation, and evaluation of clinical outcome assessments (COAs), including patient-reported outcomes (PROs), observer-reported outcomes (ObsROs), clinician-reported outcomes ...
Clinical Research Coordinator II - Psychiatry
Boston, MA · On-site
$26.50 - $35.25/hr
Preferred experience includes administering cognitive, behavioral, neuropsychological, functional, and patient-reported outcome measures; telehealth or home-based clinical research; and methods such ...
Clinical Research Coordinator II - Psychiatry
Boston, MA · On-site
$26.50 - $35.25/hr
Preferred experience includes administering cognitive, behavioral, neuropsychological, functional, and patient-reported outcome measures; telehealth or home-based clinical research; and methods such ...
Director, HTA, Value & Evidence - Obesity Early Pipeline
Manhattan, NY · On-site
$180 - $240/hr
Develop patient-reported outcomes strategies and incorporate humanistic and economic endpoints into clinical trials * Oversee customer-facing dissemination of HEOR materials in accordance with ...
Posted today
Director, HTA, Value & Evidence - Obesity Early Pipeline
Manhattan, NY · On-site
$180 - $240/hr
Develop patient-reported outcomes strategies and incorporate humanistic and economic endpoints into clinical trials * Oversee customer-facing dissemination of HEOR materials in accordance with ...
Posted today
Junior Specialist at the UC Davis Eye Center
Sacramento, CA · On-site
$55K/yr
Coordinating patient-reported outcome research studies, including survey administration and follow-up assessments. * Assisting with study start-up activities, IRB submissions/modifications, and ...
Junior Specialist at the UC Davis Eye Center
Sacramento, CA · On-site
$55K/yr
Coordinating patient-reported outcome research studies, including survey administration and follow-up assessments. * Assisting with study start-up activities, IRB submissions/modifications, and ...
$26.50 - $35.25/hr
Preferred experience includes administering cognitive, behavioral, neuropsychological, functional, and patient-reported outcome measures; telehealth or home-based clinical research; and methods such ...
$26.50 - $35.25/hr
Preferred experience includes administering cognitive, behavioral, neuropsychological, functional, and patient-reported outcome measures; telehealth or home-based clinical research; and methods such ...
The manager will work with ICCE leadership to collect, monitor, track, and improve patient-reported outcome measures (PROMs). Entity Medical University Hospital Authority (MUHA) Worker Type Employee ...
The manager will work with ICCE leadership to collect, monitor, track, and improve patient-reported outcome measures (PROMs). Entity Medical University Hospital Authority (MUHA) Worker Type Employee ...
The manager will work with ICCE leadership to collect, monitor, track, and improve patient-reported outcome measures (PROMs). Entity Medical University Hospital Authority (MUHA) Worker Type Employee ...
The manager will work with ICCE leadership to collect, monitor, track, and improve patient-reported outcome measures (PROMs). Entity Medical University Hospital Authority (MUHA) Worker Type Employee ...
Senior Director, Biostatistics
Cambridge, MA · On-site
$150 - $190/hr
Experience with blinded study designs and analyzing and interpreting patient reported outcome (PRO) data sets strongly preferred * Ability to communicate and work directly with non-statisticians ...
Senior Director, Biostatistics
Cambridge, MA · On-site
$150 - $190/hr
Experience with blinded study designs and analyzing and interpreting patient reported outcome (PRO) data sets strongly preferred * Ability to communicate and work directly with non-statisticians ...
Director, HTA, Value & Evidence - Obesity
Manhattan, NY · On-site
$180 - $240/hr
Develop patient-reported outcomes strategy and incorporate humanistic and economic endpoints into clinical trials * Provide strategic input into clinical trial designs and analyses to support ...
Posted today
Director, HTA, Value & Evidence - Obesity
Manhattan, NY · On-site
$180 - $240/hr
Develop patient-reported outcomes strategy and incorporate humanistic and economic endpoints into clinical trials * Provide strategic input into clinical trial designs and analyses to support ...
Posted today
Patient Outcome Manager
Scottsdale, AZ · On-site
$21 - $23/hr
The Patient Outcome Manager is the first therapeutic contact a patient has with the Amen Clinic and ... Perform mental status exams, score checklists and include results the prepared report. * Be able to ...
Quick apply
Patient Outcome Manager
Scottsdale, AZ · On-site
$21 - $23/hr
The Patient Outcome Manager is the first therapeutic contact a patient has with the Amen Clinic and ... Perform mental status exams, score checklists and include results the prepared report. * Be able to ...
Patient Outcome Manager
Seattle, WA · On-site
$28 - $32/hr
The Patient Outcome Manager is the first therapeutic contact a patient has with the Amen Clinic and ... Perform mental status exams, score checklists and include results the prepared report. * Be able to ...
Quick apply
Patient Outcome Manager
Seattle, WA · On-site
$28 - $32/hr
The Patient Outcome Manager is the first therapeutic contact a patient has with the Amen Clinic and ... Perform mental status exams, score checklists and include results the prepared report. * Be able to ...
$77K - $116K/yr
Leads and oversees academic research activities focused on patient reported outcome measure development and validation. Manages a team of research staff responsible for data collection, documentation ...
$77K - $116K/yr
Leads and oversees academic research activities focused on patient reported outcome measure development and validation. Manages a team of research staff responsible for data collection, documentation ...
Clinical development program support (e.g. patient-reported outcomes [PRO] strategies for clinical trials); * Real-world evidence generation (e.g. studies of natural history, burden of illness ...
Clinical development program support (e.g. patient-reported outcomes [PRO] strategies for clinical trials); * Real-world evidence generation (e.g. studies of natural history, burden of illness ...
... patient-reported outcome measures (PROMs). In addition to pursuing their own research agenda, the selected candidate will have the opportunity to collaborate with the UAB Hospital Chief Medical ...
... patient-reported outcome measures (PROMs). In addition to pursuing their own research agenda, the selected candidate will have the opportunity to collaborate with the UAB Hospital Chief Medical ...
Clinical development program support (e.g. patient-reported outcomes [PRO] strategies for clinical trials); * Real-world evidence generation (e.g. studies of natural history, burden of illness ...
Clinical development program support (e.g. patient-reported outcomes [PRO] strategies for clinical trials); * Real-world evidence generation (e.g. studies of natural history, burden of illness ...
Director, Respiratory Biologics - Global Real-World Evidence & Health Outcomes Research
Concord, NC · On-site +1
Masters in health outcomes, patient reported outcomes, health economics, epidemiology, pharmacy, health or life sciences. * 10 + years' experience working in pharmaceutical industry, preferably in a ...
Director, Respiratory Biologics - Global Real-World Evidence & Health Outcomes Research
Concord, NC · On-site +1
Masters in health outcomes, patient reported outcomes, health economics, epidemiology, pharmacy, health or life sciences. * 10 + years' experience working in pharmaceutical industry, preferably in a ...
... patient-reported outcome measures such as quality-of-life endpoints, including handling of missing data such as that due to non-response, death, or other intercurrent events. • Demonstrated ...
... patient-reported outcome measures such as quality-of-life endpoints, including handling of missing data such as that due to non-response, death, or other intercurrent events. • Demonstrated ...
Director, Respiratory Biologics - Global Real-World Evidence & Health Outcomes Research
Philadelphia, PA · On-site +1
Masters in health outcomes, patient reported outcomes, health economics, epidemiology, pharmacy, health or life sciences. * 10 + years' experience working in pharmaceutical industry, preferably in a ...
Director, Respiratory Biologics - Global Real-World Evidence & Health Outcomes Research
Philadelphia, PA · On-site +1
Masters in health outcomes, patient reported outcomes, health economics, epidemiology, pharmacy, health or life sciences. * 10 + years' experience working in pharmaceutical industry, preferably in a ...
Director, Respiratory Biologics - Global Real-World Evidence & Health Outcomes Research
Upper Providence, PA · On-site
Masters in health outcomes, patient reported outcomes, health economics, epidemiology, pharmacy, health or life sciences. * 10 + years' experience working in pharmaceutical industry, preferably in a ...
Director, Respiratory Biologics - Global Real-World Evidence & Health Outcomes Research
Upper Providence, PA · On-site
Masters in health outcomes, patient reported outcomes, health economics, epidemiology, pharmacy, health or life sciences. * 10 + years' experience working in pharmaceutical industry, preferably in a ...
Director, Respiratory Biologics - Global Real-World Evidence & Health Outcomes Research
Upper Providence, PA · On-site +1
Masters in health outcomes, patient reported outcomes, health economics, epidemiology, pharmacy, health or life sciences. * 10 + years' experience working in pharmaceutical industry, preferably in a ...
Director, Respiratory Biologics - Global Real-World Evidence & Health Outcomes Research
Upper Providence, PA · On-site +1
Masters in health outcomes, patient reported outcomes, health economics, epidemiology, pharmacy, health or life sciences. * 10 + years' experience working in pharmaceutical industry, preferably in a ...
Patient Reported Outcome information
See salary details
$10.10 - $14.90
5% of jobs
$14.90 - $19.71
16% of jobs
$22.72 is the 25th percentile. Wages below this are outliers.
$19.71 - $24.52
6% of jobs
$24.52 - $29.33
4% of jobs
$29.33 - $34.13
2% of jobs
$34.13 - $38.94
1% of jobs
The median wage is $41.62 / hr.
$38.94 - $43.75
27% of jobs
$45.71 is the 75th percentile. Wages above this are outliers.
$43.75 - $48.56
32% of jobs
$48.56 - $53.37
6% of jobs
$53.37 - $58.17
0% of jobs
$58.17 - $62.98
0% of jobs
$10
$37
$62
How much do patient reported outcome jobs pay per hour?
What is a patient reported outcome?
A Patient Reported Outcome (PRO) job involves collecting, analyzing, and interpreting data reported directly by patients about their health conditions, treatment experiences, and quality of life. Professionals in this role work in clinical research, healthcare, or pharmaceutical industries to ensure patient feedback informs medical decisions and regulatory approvals. They may develop surveys, assess data validity, and collaborate with stakeholders to improve patient care. The goal is to enhance healthcare outcomes by incorporating the patient’s perspective into research and treatment evaluations.
What are the typical responsibilities of a patient reported outcome professional?
Professionals in Patient Reported Outcome (PRO) roles are responsible for designing, implementing, and analyzing patient surveys and questionnaires to capture patient perspectives during clinical trials or healthcare studies. They often collaborate with clinical teams, data managers, and regulatory specialists to ensure that collected data meet quality standards and regulatory requirements. Their day-to-day tasks may include managing electronic PRO systems, training study staff, reviewing data integrity, and preparing reports for study sponsors or regulatory bodies. This role offers the opportunity to make a direct impact on how patient experiences shape clinical research and healthcare decision-making.
What are the key skills and qualifications needed for a patient reported outcome role?
To thrive in a Patient Reported Outcome (PRO) role, you typically need a background in healthcare, research, or data analysis, along with strong knowledge of clinical study design and patient-centered outcome measures. Expertise in data capture and management platforms (such as ePRO/eCOA systems), familiarity with regulatory guidelines, and sometimes certifications like Certified Clinical Research Professional (CCRP) are highly valued. Attention to detail, strong communication, and the ability to collaborate across multidisciplinary teams are crucial soft skills. These competencies ensure accurate data collection, regulatory compliance, and the effective translation of patient experiences into actionable insights for healthcare improvement.
What cities are hiring for Patient Reported Outcome jobs?
Cities with the most Patient Reported Outcome job openings:
What are the most commonly searched types of Patient Reported Outcome jobs?
The most popular types of Patient Reported Outcome jobs are:
What states have the most Patient Reported Outcome jobs?
States with the most job openings for Patient Reported Outcome jobs include:
What job categories do people searching Patient Reported Outcome jobs look for?
The top searched job categories for Patient Reported Outcome jobs are:

Full-time
Medical, Dental, Life, Retirement, PTO
Re-posted 2 days ago
RTI International rating
7.0
Based on 5 frontline employees who took The Breakroom Quiz
62nd of 73 rated research
Job description
RTI Health Solutions (RTI-HS), a wholly owned subsidiary of RTI International, is an independent and internationally recognized research organization. With offices in the US, UK, Spain, France, and Sweden, we provide healthcare consulting and research expertise to optimize decision making for pharmaceutical, biotechnology, and medical device products across the development and marketing lifecycle. Clients rely on our expertise, quality standards, and integrity to guide their product development and regulatory and market access strategies. Our various practice areas include Value, Access, and HEOR; Patient-Centered and Outcomes Research; Epidemiology and Biostatistics; Medical Communications; Global Business Operations; and Strategic Consulting and Growth.
RTI Health Solutions is seeking an experienced and highly collaborative Senior Scientist to join our Patient-Centered Outcomes Assessment (PCOA) team. This role is ideal for a senior researcher who thrives at the intersection of hands-on execution, scientific leadership, and collaboration.
As a senior member of the PCOA team, you will lead multidisciplinary project teams while remaining actively engaged in the design, conduct, analysis, interpretation, and dissemination of patient-centered research. You will serve as both a scientific leader and a working manager-providing strategic direction, mentoring staff, and ensuring project success while directly contributing to high-impact client deliverables.
You will partner with pharmaceutical and biotechnology clients to generate patient-centered evidence throughout the drug development lifecycle, supporting regulatory, reimbursement, and market access objectives.
What You'll Do
Key Responsibilities
Project and Scientific Leadership
- Lead complex patient-centered outcomes research programs from study design through final delivery.
- Serve as project lead for multidisciplinary teams, ensuring projects are delivered on time, within scope, and to the highest scientific standards.
- Provide strategic oversight of study design, methodology, regulatory engagement, and evidence generation plans.
- Manage project risks, client expectations, resource allocation, and team performance.
- Serve as a trusted scientific advisor to clients and internal stakeholders.
Research Execution and Technical Contribution
- Personally contribute to the design, execution, analysis, interpretation, and reporting of qualitative and mixed-methods research studies.
- Design and lead qualitative research conducted with patients, caregivers, patient advocates, and clinical key opinion leaders, including both stand-alone and clinical trial-based studies.
- Lead the development, adaptation, and evaluation of clinical outcome assessments (COAs), including patient-reported outcomes (PROs), observer-reported outcomes (ObsROs), clinician-reported outcomes (ClinROs), and related measures.
- Review and critically appraise published literature, COA development programs, and psychometric evidence.
- Develop patient-centered evidence strategies to support regulatory, access & reimbursement, and healthcare decision-making needs.
- Contribute directly to study reports, client presentations, evidence dossiers, briefing books, and negotiations with key decision makers to support patient-centered value messaging for medicines.
Client Leadership and Business Development
- Build and maintain strong relationships with existing and prospective clients.
- Lead scientific discussions with pharmaceutical and biotechnology sponsors regarding patient-focused drug development strategies.
- Support business development efforts through proposal development, client meetings, capability presentations, and identification of growth opportunities.
- Contribute to strategic planning and expansion of RTI-HS PCOA capabilities.
Publications, Dissemination, and Thought Leadership
- Lead and contribute to scientific publications, conference abstracts, posters, presentations, and manuscripts.
- Represent RTI-HS at scientific meetings, industry conferences, and client engagements.
- Stay current with evolving regulatory guidance, methodological advancements, and industry best practices in patient-centered outcomes research.
People Leadership and Talent Development
- Provide day-to-day leadership, mentorship, and coaching to junior and mid-level researchers.
- Foster technical excellence, knowledge sharing, and professional development across project teams.
- Support staff development through project leadership opportunities, scientific review, and career mentoring.
- Contribute to building a collaborative, inclusive, and high-performing team culture.
What You'll Need
- A postgraduate master's level degree plus a minimum of 8 years of experience conducting patient-centered research, or a PhD plus a minimum of 5 years of experience conducting patient-centered research.
- Demonstrated experience leading complex patient-centered research projects and multidisciplinary teams within a consulting, pharmaceutical, regulatory, CRO, or academic research environment supporting patient-focused drug development.
- Demonstrated success managing client relationships, mentoring research staff, and leading project teams.
- Substantial experience developing and successfully executing patient-centered evidence-generation strategies for pharmaceutical clients.
- Proven experience interacting with regulatory agencies, including FDA, EMA, or other global health authorities as well as supporting evidence needs for access stakeholders (payers HTA, and prescribers) .
- Experience leading proposal development and contributing to business growth initiatives.
- Strong publication record and experience presenting research at scientific conferences.
#LI-BM1
EEO & Pay Equity Statements
For San Francisco, CA USA Job Postings Only: Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Further information is available here.
RTI accepts applications to our job openings from candidates with criminal histories or conviction records in accordance with all applicable laws, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
For Applicants in Massachusetts Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
The anticipated pay range for this role is listed below. Our pay ranges represent national averages and may vary by location as a geographic differential may be applied to some locations within the United States. RTI considers multiple factors when making an offer including, for example: established salary range, internal budget, business needs, and education and years of work experience possessed by the applicant. Further, salary is merely one element to our offer.
At RTI, we demonstrate our commitment to rewarding individual and team achievement through a total rewards package. This package includes (among other things) a competitive base salary, a generous paid time off policy, merit based annual increases, bonus opportunities and a robust recognition program. Other benefits include a competitive range of insurance plans (including health, dental, life, and short-term and long-term disability), access to a retirement savings program such as a 401(k) plan, paid parental leave for all parents, financial assistance with adoption expenses or infertility treatments, financial reimbursement for education and developmental opportunities, an employee assistance program, and numerous other offerings to support a healthy work-life balance.
Hiring Salary Range
$150,000.00-$250,000.00
What RTI International employees say
Pay
Hours and flexibility
Workplace
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About RTI International
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
1,001 - 5,000 Employees
Headquarters location
Durham, NC, US
Year founded
1958