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

Two computer monitors with data graphs
How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish date

12/01/2025

Summary

How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i

Teaser label

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

Read more
Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish date

11/28/2025

Summary

Quality and Compliance for New Entrants:           A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

Read more
Female using a laptop to search for jobs
Improving Your Visibility in the Clinical Research Job Market

Teaser label

Career Progression

Content type

Blogs

Publish date

11/26/2025

Summary

How Clinical Research Job Seekers Can Enhance Their Applications Finding the right role in clinical research has become increasingly competitive as organisations continue to expand their study por

Teaser label

Discover the search terms recruiters use most often and practical steps that can help candidates strengthen their visibility.

Read more
View all

Similar jobs at ICON

Clinical Data Science Programmer

Salary

Location

Colombia, Bogota

Location

Bogota

Mexico City

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Programming

Job Type

Permanent

Description

We are currently seeking a Clinical Data Science Programmer to join our diverse and dynamic team. As a Clinical Data Science Programmer at ICON, you will play an essential role in developing and imple

Reference

JR137209

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Senior Specialist, Publications Operations

Salary

Location

Canada, Burlington

Location

Canada

Montreal

Burlington

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

The Publications Operations Senior Specialist is responsible for providing operational and administrative support to Publication Managers within the Publication Operations Team in Global Medical Affai

Reference

JR140391

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Sr. CRA - São Paulo (FSP - Sponsor Dedicated)

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON Plc, you will play a critical role in overseeing and managing clin

Reference

JR140016

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
CRA I or II

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

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

JR139582

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
CRA Careers in Italy

Salary

Location

Italy, Milan

Location

Milan

Remote Working

Office Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

From early-stage development to post-approval studies and commercialization strategies, our comprehensive services enable our partners to navigate the complex regulatory landscape and accelerate their

Reference

JR140389

Expiry date

01/01/0001

Read more Shortlist Save this role
CRA I or II - São Paulo

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordina

Reference

JR140064

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above