JUMP TO CONTENT

(Senior) Principal Scientist, Patient Centered Outcomes

052351_2

About the role

This vacancy has now expired. Please click here to view live vacancies.

ICON plc is looking for a Principal Scientist – Patient Centered Outcomes to join our winning team named by Forbes as one of the best large employers in America for the year 2018. We are a top five clinical research organization with stability, solid earnings and growth potential with 13,500 employees in forty countries globally.

You will join ICON’s Patient-Centered Outcomes (PCO) group which sits within ICON's Commercialization and Outcomes division, a market leader providing a range of services to the Pharmaceutical and Medical Device markets spanning Health Economics, Epidemiology, PCO, Pricing & Market Access, Translations and Linguistic Validation, Medical Communications and Real World Evidence.

ICON’s PCO group provides services geared to meet the demands of global and national markets for high quality patient-centered data. Our PCO group brings together a large team of Outcomes Research scientists and consultants with expertise in the selection, development, validation and analysis of Patient Reported Outcome (PRO) and other Clinical Outcomes Assessment (COA) instruments. The group has a deep understanding of the marketplace and regulatory landscapes, and helps decision-makers to understand the value of patient-centered endpoints and to estimate the impact of new health technologies.

 

Overview of the role

The Principal Scientist will have a leadership position in our growing team and will serve as the project director and/or scientific advisor for projects, taking responsibility for the scientific integrity of the research.  The Principal also supports the overall business strategy. 

 

To succeed you will need

·         Significant academic or industry experience in patient-centered/ reported outcomes research.  

·         Applied knowledge of both qualitative and quantitative research methods

·         Experience of writing study protocols, statistical analysis plans, and study reports

·         Ability to coach/mentor junior staff in the application of research methods

·         Experience in the use and application of  both qualitative and quantitative software packages

·         Experience with regulatory bodies including the EMA and FDA.

·         Proficiency in MS Word, PowerPoint, and Excel

  • Experience of leading outcomes research studies and directing project teams
  • Strong analytical and problem-solving skills
  • Comprehensive understanding of health outcomes research principles and familiarity with key aspects of the literature (historical and current)
  • Excellent communication and scientific writing skills, as demonstrated by peer-reviewed publications, technical reports, or other scholarly work
  • Ability to act as COA functional lead in cross-functional teams
  • Ability to manage own workload with respect to project scope, timelines and quality
  • Ability to travel (approximately 20%) domestic and/or international

Working for ICON you will be provided with an excellent benefits package. We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.   

 

ICON plc Company is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment. #LI-AA1

List #1

Day in the life

Headshot of male
25 Years in Clinical Operations at ICON: Ricardo Cortizo Justo Q&A

Teaser label

Our People

Content type

Blogs

Publish 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

Ricardo shares insights from 25 years at ICON, covering clinical operations, leadership, and career development.

Read more
Heartbeat vitals on monitor
Central Monitoring vs On Site Monitoring

Teaser label

Industry

Content type

Blogs

Publish 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

Learn the difference between central monitoring and on site monitoring and how both support patient safety and data quality.

Read more
middle aged male wearing shirt
Francis' Journey back to ICON

Teaser label

Our People

Content type

Blogs

Publish 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

Teaser label

Francis Kayamba shares what drew him back to ICON and how the sponsor-embedded model works.

Read more
View all

Similar jobs at ICON

Senior Clinical Research Associate

Salary

Location

Singapore, Singapore

Location

Singapore

Kuala Lumpur

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

JR148701

Expiry date

01/01/0001

Maria Clare

Author

Maria Clare
Maria Clare

Author

Maria Clare
Read more Shortlist Save this role
Clinical Data Coordinator

Salary

Location

India, Chennai

Location

Chennai

Remote Working

Hybrid

Business Area

ICON Strategic Solutions

Job Categories

Clinical Data Management

Job Type

Permanent

Description

We are currently seeking a Clinical Data Coordinator II to join our diverse and dynamic team. As a Clinical Data Coordinator II at ICON, you will play a pivotal role in designing and analyzing clinica

Reference

JR142313

Expiry date

01/01/0001

Abhisikta Mishra Read more Shortlist Save this role
Proposals Development Associate II

Salary

Location

UK, Reading

Department

Full Service - Commercial Solutions

Location

Dublin

Reading

Swansea

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Proposals

Job Type

Permanent

Description

Proposals Development AssociateLocation: UK/IrelandAbout the Proposals Development Associate:The Proposals Development Associate II is responsible for supporting business development in the winning of

Reference

JR148255

Expiry date

01/01/0001

Caroline Lock

Author

Caroline Lock
Read more Shortlist Save this role
Study Start-Up Manager

Salary

Location

Australia, Sydney

Location

Sydney

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

Role: Study Start-Up LeadLocation: Australia - home-based  Join ICON Strategic Solutions, embedded within a globally recognised, science-driven biopharmaceutical organisation at the forefront of innov

Reference

JR148232

Expiry date

01/01/0001

Krisztina Auth Read more Shortlist Save this role
Senior Regulatory Submission Specialist

Salary

Location

Australia, Sydney

Location

Sydney

Auckland

Remote Working

Remote or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Regulatory Affairs

Job Type

Permanent

Description

Senior Regulatory Submission SpecialistLocation: Home-based in Australia or New Zealand Join a global leader shaping the future of clinical researchAt ICON, we’re driven by a simple purpose: to improv

Reference

JR140743

Expiry date

01/01/0001

Krisztina Auth Read more Shortlist Save this role
Clinical Research Associate 2

Salary

Location

Malaysia, Kuala Lumpur

Location

Kuala Lumpur

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli

Reference

JR147769

Expiry date

01/01/0001

Leslie Garcia

Author

Leslie Garcia
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above