Our Clinical Research Associates (CRAs) are at the heart of our success
CRA’s work closely with pharmaceutical companies, clinical contractors and hospitals, ensuring adherence to regulations and principles from phases II-IV of a clinical trial. Our CRAs are at the core of everything we do at ICON. They work closely together with our customers to tackle complex issues that can improve the health of patients and the care they receive.
CRAs are often referred to as Monitors and this is the key difference between a CRA and a clinical research coordinator (CRC). While CRAs are responsible for overseeing a trial and ensuring compliance, CRCs see to patient consenting, identifying patients and reporting adverse effects in clinical trials.
Browse our available Clinical Research Associate Jobs below, or sign up for alerts to be notified when suitable vacancies arise.
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Day in the Life of a CRA at ICON
In this video, Linh Ngoc Huynh, CRA II at ICON shares a behind-the-scenes look at a typical day in the life of a CRA.
Whether you're an experienced CRA or considering your first step into clinical operations, this video offers valuable insight into how we support your growth, empower you to do meaningful work, and help you build a rewarding career.
Inside ICON
Inside ICON - Blogs
CRA vs CRC
The difference between a CRA & In-house CRA
What role will a CRA play in future Clinical Trials?
Becoming a CRA at ICON: Cissy's Story
Salary
Location
Regional Norway
Location
Norway
Remote Working
Remote
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
JR144562
Expiry date
01/01/0001
Read more
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Salary
Location
France, Paris
Location
Paris
Remote Working
Remote
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
JR144544
Expiry date
01/01/0001
Read more
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Salary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
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
JR144563
Expiry date
01/01/0001
Read more
Shortlist Save this role
Salary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
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
JR144565
Expiry date
01/01/0001
Read more
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Salary
Location
Italy, Milan
Location
Milan
Remote Working
Remote
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
JR144558
Expiry date
01/01/0001
Read more
Shortlist Save this role
Salary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a CRA to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting com
Reference
JR139873
Expiry date
01/01/0001
Read more
Shortlist Save this role
Salary
Location
France, Paris
Location
Paris
Remote Working
Remote
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
JR145563
Expiry date
01/01/0001
Read more
Shortlist Save this role
Salary
Location
Brazil, Sao Paulo
Department
Clinical Monitoring
Location
Sao Paulo
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking CRAs II and Senior CRAs to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials
Reference
JR146108
Expiry date
01/01/0001
Read more
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Salary
Location
Regional United States (PRA)
Department
Clinical Monitoring
Real World Solutions
Location
Multiple US Locations
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II or Senior CRAs to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing an
Reference
JR145857
Expiry date
01/01/0001
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Salary
Location
Chicago, IL
Location
Indianapolis, IN
Chicago, IL
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess sit
Reference
JR146514
Expiry date
01/01/0001
Read more
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Salary
Location
US, Raleigh, NC
Location
Raleigh
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess sit
Reference
JR146510
Expiry date
01/01/0001
Read more
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Salary
Location
Basking Ridge, NJ
Location
Basking Ridge, NJ
Chadds Ford, PA
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess sit
Reference
JR146507
Expiry date
01/01/0001
Read more
Shortlist Save this role
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Teaser label
IndustryContent type
BlogsPublish date
02/16/2026
Summary
What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh
Teaser label
IndustryContent type
BlogsPublish date
02/16/2026
Summary
Functional Service Provision (FSP), also known as sponsor-embedded delivery, is a core part of how modern clinical research is delivered. At ICON Strategic Solutions, our teams work as an extens
Teaser label
Our PeopleContent type
BlogsPublish date
02/05/2026
Summary
Building expertise through diverse roles and continuous learning Sinéad McKeon's career at ICON demonstrates how scientific training can evolve into strategic leadership. Now a Senior Manager in Lab