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
China, Shanghai
Location
Shanghai
Hangzhou
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Job Advert PostingAt ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’
Reference
JR152669
Expiry date
01/01/0001
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Salary
Location
Argentina, Buenos Aires
Department
Clinical Monitoring
Location
Buenos Aires
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking CRAs II & Senior CRAs (Sponsor-Dedicated / Multisponsor) to join our diverse and dynamic team. You will play a pivotal role in designing and analyzing clinical trials, interpr
Reference
JR140950
Expiry date
01/01/0001
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Salary
Location
Brazil, Sao Paulo
Department
Clinical Monitoring
Real World Solutions
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
JR150677
Expiry date
01/01/0001
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Salary
Location
US, Downers Grove, IL
Department
Clinical Monitoring
Location
Portland
Salt Lake City
Houston
Downers Grove
Lawrence
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and dynamic team. As a CRA II/Senior CRA at ICON, you will play a pivotal role in designing and analyzin
Reference
JR153618
Expiry date
01/01/0001
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Salary
Location
Sweden, Lund
Department
Clinical Monitoring
Real World Solutions
Location
Copenhagen
Lund
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will
Reference
JR152930
Expiry date
01/01/0001
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Salary
Location
Romania, Bucharest
Department
Clinical Monitoring
Location
Bucharest
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II or Senior CRA at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Wil
Reference
JR149899
Expiry date
01/01/0001
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Salary
Location
China, Beijing
Location
Beijing
Remote Working
Office Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will
Reference
JR154983
Expiry date
01/01/0001
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Salary
Location
China, Shanghai
Location
Shanghai
Remote Working
Office Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will
Reference
JR155004
Expiry date
01/01/0001
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Salary
Location
Malaysia, Kuala Lumpur
Location
Kuala Lumpur
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA I at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will c
Reference
JR154225
Expiry date
01/01/0001
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Salary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
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
JR154870
Expiry date
01/01/0001
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Salary
Location
Tampa, FL
Location
Atlanta
Jacksonville, FL
Miami, FL
Tampa, FL
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 site
Reference
JR154201
Expiry date
01/01/0001
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Salary
Location
Washington DC
Location
Virginia
Washington DC
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 site
Reference
JR147406
Expiry date
01/01/0001
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Teaser label
Our PeopleContent type
BlogsPublish date
06/10/2026
Summary
Why I Still Recommend the CTA Role After More Than 10 Years in Clinical Research Clinical Operations Manager Yordan Zahariev reflects on career growth, leadership and the opportunities a CTA role
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Teaser label
Our PeopleContent type
BlogsPublish date
06/04/2026
Summary
After more than 20 years at ICON, Carolina Boari has witnessed the organisation's growth across Latin America while building a successful career of her own. Today, as Executive Director of Clini
Teaser label
Our PeopleContent type
BlogsPublish date
05/26/2026
Summary
From Data Management to Leadership For Sajna Basant, a career in Biometrics has always been about more than data. “Data is not just numbers,” she explains. “It represents real people, their health