Outcomes Researcher- Quantitative
About the role
This vacancy has now expired. Please click here to view live vacancies.
Outcomes Researcher- Quantitative
ICON Patient Centred Outcomes is currently seeking a Research Consultant/ Outcomes Researcher (Psychometrics, quantitative) to join our team!
Location - EU wide (flexible to be home/office based)
ICON Patient Centred Outcomes (PCO) is part of ICON plc, a leading global Clinical Research Organization headquartered in Dublin, Ireland. Our PCO group undertakes consultancy projects for international clients in both the pharmaceutical and medical device sectors, supporting late-phase clinical trials.
The work of the PCO group focuses on patient-centered research, including health related quality of life, disease signs and symptoms, treatment preference, adherence and satisfaction. The group is respected globally for the quality and innovation of their applied qualitative and quantitative work. Much of their work involves Clinical Outcome Assessment (COA) endpoint/instrument selection and regulatory support; COA instrument development and psychometric validation; study design, analysis and interpretation; COA quantitative analysis; utility measurement; and patient preference studies. Our PCO team is based in US (San Francisco, Boston, Gaithersburg, Raleigh), UK, France (Lyon) and Germany.
We are looking for an individual who is looking to join a consultancy group where research experience is applied within a fast-moving commercial environment. In particular, we are looking for someone who is looking to apply their quantitative skills and join our growing quantitative team.
You will have experience of applied research in an academic or commercial environment, and will have experience of, and interest in, research study design and interpretation of results, psychometric evaluation of COA instruments, analysis of COA data from a range of study designs, and of using statistical software packages (e.g. Stata, SAS, R).
You will also have experience of providing leadership and guidance to more junior staff members and of managing both projects and research teams, including day-to-day liaison with clients. You will also need to be capable of contributing to publications/scientific communications, to demonstrate and actively promote an open and honest working environment, encourage close teamwork and foster knowledge transfer.
The ideal candidate will possess:
- Bachelor's degree, or local equivalent in a related field (such as public health, epidemiology, biostatistics, or related discipline). Post-graduate qualification in a related field preferred (e.g. MSc, PhD/DPhil, Clinical).
- Experience of both conducting health research and managing research projects.
- Experience of working in a healthcare/consultancy environment.
- Demonstrable experience of quantitative research and related technical skills.
- Excellent oral and written communication skills.
- Accuracy and attention to detail.
- The ability to work effectively as part of a team with a high degree of self-motivation.
- Development and Leadership potential.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
04/08/2026
Summary
Ricardo Cortizo Justo, Director of Clinical Operations and Site Head for Paris at ICON plc, recently marked an exceptional milestone of 25 years with the organisation. Over the course of his career, R
Teaser label
IndustryContent type
BlogsPublish date
04/03/2026
Summary
Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re
Teaser label
Our PeopleContent type
BlogsPublish date
03/26/2026
Summary
Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February
Similar jobs at ICON
Salary
Location
Chile, Santiago
Location
Santiago
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
Clinical Trial Manager (FSP - Sponsor Dedicated) We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for
Reference
JR147030
Expiry date
01/01/0001
Author
Elizabeth DaviesAuthor
Elizabeth DaviesSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Hybrid
Business Area
ICON Strategic Solutions
Job Categories
Accounting & Finance
Job Type
Permanent
Description
We are currently seeking an Investigator Pricing Analyst to join our diverse and dynamic team. As an Investigator Pricing Analyst at ICON, you will play a pivotal role in determining fair market value
Reference
JR142489
Expiry date
01/01/0001
Author
Rita VillavicencioAuthor
Rita VillavicencioSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Senior Pharmacovigilance Associate to join our diverse and dynamic team. As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and
Reference
JR145501
Expiry date
01/01/0001
Author
Rita VillavicencioAuthor
Rita VillavicencioSalary
Location
US, Blue Bell (ICON)
Location
Burlington
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Project Management
Job Type
Permanent
Description
As a TDM at ICON, you will be responsible for leading and coordinate project activities, ensuring that projects are delivered on time, within budget, and to the highest quality standards.What You Will
Reference
JR148315
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
Brazil, Sao Paulo
Location
Buenos Aires
Sao Paulo
Bogota
Lima
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Liaison
Job Type
Permanent
Description
We are currently seeking a Trilingual Clinical Trial Enrollment Liaison to join our diverse and dynamic team. As a Clinical Trial Enrollment Liaison at ICON, you will play a pivotal role in designing
Reference
JR145938
Expiry date
01/01/0001
Author
Olivia MolinaAuthor
Olivia MolinaSalary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:
Reference
JR148555
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie Pruitt