CTA
About the role
This vacancy has now expired. Please click here to view live vacancies.
This is an exciting opportunity to join ICON
ICON, a leading Clinical Research Organization, is seeking passionate, resilient and inspiring Graduates to join our team as a Clinical Trial Assistant. This opportunity offers an entry-level permanent position to highly skilled individuals interested in a career in clinical research.
We empower our Clinical Trial Assistants to work with a collaborative and successful team to support our Clinical Trial Management and Project Management teams with operational activities. They provide administrative support to various projects, maintain and track clinical study documentation, coordinate study materials, and collate relevant study information.
This unique opportunity is designed for individuals with a Bachelor's Degree in Life Sciences, strong organizational skills, excellent written and verbal communication, and working knowledge of computer systems including Microsoft Word, Excel, Outlook, and PowerPoint.
We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.
There is no limit to what you can achieve at ICON. From contributing to the development of life-saving drugs to working in a team of dedicated experts, your work is always valued. Teamwork is actively encouraged! We value commitment to excellence and promote this across every element of our business. Our Clinical Trial Assistants are engaged and motivated to do their best every day.
Working for ICON you will be provided with a comprehensive benefits package including competitive salary, bonus, 401K with employer match, generous PTO and paid holidays.
ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
Benefits of Working in ICON :
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
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 is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
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
IndustryContent type
BlogsPublish 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
IndustryContent type
BlogsPublish 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
Career ProgressionContent type
BlogsPublish 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
Similar jobs at ICON
Salary
Location
UK, Reading
Location
Reading
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON, you will play a critical role in overseeing and managing clinical tri
Reference
JR138809
Expiry date
01/01/0001
Author
Sophie BinghamAuthor
Sophie BinghamSalary
Location
Romania, Bucharest
Location
Bucharest
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking experienced Clinical Research Associates with previous experience in oncology to join our diverse and dynamic FSP team in Romania.As a Clinical Research Associate at ICON Plc,
Reference
JR139956
Expiry date
01/01/0001
Author
Dariusz SternlichtAuthor
Dariusz SternlichtSalary
Location
United States of America
Department
Clinical Monitoring
Real World Solutions
Location
Multiple US Locations
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Clinical Site Associate (CSA) Open to candidates located anywhere in the USA. We are currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team. As a CSA at ICON, you will
Reference
JR139929
Expiry date
01/01/0001
Author
Jypson Jose
Author
Jypson JoseSalary
Location
Regional United States (PRA)
Location
Multiple US Locations
Portland
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug / Device Regulatory Affairs
Job Type
Permanent
Description
Sr Manager, Regulatory Affairs – IVDLocation: US Remote, Portland, OR area preferredWe are currently seeking a Senior Manager, Regulatory Affairs to join our diverse and dynamic team. As a Senior Mana
Reference
JR137759
Expiry date
01/01/0001
Author
Sasha BrownAuthor
Sasha BrownSalary
Location
US, Blue Bell (ICON)
Department
Full Service - Development & Commercialisation Solutions
Location
Dublin
Blue Bell
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Quality Assurance
Job Type
Permanent
Description
We are currently seeking a Clinical Quality Compliance Lead to join our diverse and dynamic team. As a Clinical Quality Compliance Lead at ICON, you will play a pivotal role in designing and analyzing
Reference
JR136890
Expiry date
01/01/0001
Author
Sasha BrownAuthor
Sasha BrownSalary
Location
Poland, Warsaw
Department
Full Service - Corporate Support
Location
Mexico City
Sofia
Dublin
Warsaw
Bangalore
Chennai
Trivandrum
Bengaluru
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Facilities & Administratives Services
Job Type
Permanent
Description
Role Overview We are seeking a highly skilled Manager, Business Continuity to join our team and help ensure ICON is prepared to respond effectively to business interruptions. You will collaborate with
Reference
JR137815
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda Kozuszek