Job Description

We encourage our people to seize the opportunity to bring flexibility, innovation and determination to every situation.
By doing this, our people build exciting and rewarding careers, deliver results to help bring life-changing medicines and devices to market and maintain ICON's success as an industry leader.
Full Service
Full-service roles offer the opportunity to work on projects and programmes on behalf of the world's most innovative pharma, biotech and medical device companies.
ICON Strategic Solutions
Our Strategic Solutions team is embedded in our clients' businesses, helping to deliver cutting edge research.
Global Business Services
Global Business Services functions are the backbone of the organisation, providing support services in areas including Finance, IT, HR, Sales, QA, Facilities & Administration, Legal & Procurement.
Commercial roles offer opportunities to be involved in the exciting world of proposals, sales and marketing. * Inside ICON

• Our Locations

Our Locations
With headquarters in Dublin, Ireland, ICON has employees in 119 locations across 53 countries.

• Why ICON?

Why ICON?
No matter what part of ICON you work in, you are contributing to solving some of the most complex healthcare challenges and are helping to deliver new medicines and devices that are impacting millions of peoples' lives, right across the world.
Events? full service mean for you?
Integer posuere erat a ante venenatis dapibus posuere velit aliquet. Duis mollis, est non commodo luctus, nisi erat porttitor ligula. * Early Talent
Early Talent
Early talent programs are designed to provide participants with opportunities to gain valuable experience, develop their skills, and build relationships with experienced leaders within the organization. Early talent programs can take many forms, including internships, academy programs, and leadership development programs. ICON is committed to recruiting top talent while also fostering a culture of learning and development within the organization.
graduate What does full service mean for you?
Integer posuere erat a ante venenatis dapibus posuere velit aliquet. Duis mollis, est non commodo luctus, nisi erat porttitor ligula.
Clinical Trial Associate

• Location:

Burlington
Reference: JR143479

• Categories

Clinical Trial Support * __vacancyopjusttionswidget.opt-Business Area__
ICON Strategic Solutions * __vacancyopjusttionswidget.opt-Remote Working __
Remote
Senior Talent Acquisition Business Partner
Email
Send me a message
First Name*
Last Name*
()[].,;:s@"]+(.[^
()\[]\.,;:s@"]+)*)|(".+"))@(([[0-9]{1,3}.[0-9]{1,3}.[0-9]{1,3}.[0-9]{1,3}])|(([a-zA-Z-0-9]+.)+[a-zA-Z]{2,}))$" data-required="true" id="emailinput" maxlength="256" name="emailinput" placeholder="Email address" type="text">Email address*
Enquiry*
About the role
Clinical Trial Associate
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a CTA to join our diverse and dynamic team. As a CTA at ICON, you will play a critical role in overseeing site management activities, ensuring the smooth operation of clinical trials at the site level. You will work closely with clinical teams, providing guidance and support to ensure that sites meet regulatory and operational requirements while delivering high-quality data and achieving study goals.
What You Will Be Doing:
Overseeing day-to-day site management activities, ensuring that clinical trial sites comply with study protocols, regulatory requirements, and timelines.
Collaborating with site staff and cross-functional teams to resolve issues, monitor progress, and ensure timely data collection and reporting.
Assisting with site initiation, monitoring visits, and close-out activities to ensure the proper execution of clinical trials.
Providing guidance and mentorship to junior site management staff, fostering collaboration and process improvement.
Preparing and maintaining site management documentation, including site reports, communications, and updates on site performance.
Your Profile:
Bachelor's degree in life sciences, clinical research, or a related field.
Extensive experience in site management, clinical operations, or monitoring within the clinical research industry.
Strong understanding of clinical trial processes, Good Clinical Practice (GCP), and regulatory requirements.
Excellent problem-solving and organizational skills, with the ability to manage multiple sites and timelines.
Effective communication and interpersonal skills, with a focus on collaboration and maintaining strong site relationships.
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click to apply
Share:
ICON and you
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.
List #1
Day in the life
Teaser label
Content type
Publish date
01/26/2023
Summary
The CRO market has seen an unmistakable uplift in demand for its services in recent years. The call for personalised medicine, pricing pressures, and increasing complexity in clinical trials a
Teaser label
The CRO market has seen an unmistakable uplift in demand for its services in recent years.
Teaser label
Content type
Publish date
10/03/2022
Summary
In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the
Teaser label
In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics. This is subject to change with an increase in decentralised clinical trials (DCTs).
Teaser label
Content type
Publish date
05/22/2022
Summary
Having enjoyed steady growth over the last several years, it's predicted that the global clinical trials market will hit a value of $65.2 billion by 2025, and around 58% of this can be attribute
Teaser label
Have you ever wondered what's involved in a clinical trial? In this blog post, we take you through each distinct phase.
Similar jobs at ICON
Salary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Trial Associate (CTA) to join our diverse and dynamic team, supporting a dedicated sponsor. As a Senior CTA you will play a key role in supporting the manage
Reference
JR142664
Expiry date
01/01/0001
Author
Author
Salary
Location
Romania, Bucharest
Location
Sofia
Bucharest
Belgrade
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are looking for candidates with experience in global study management supporting global project managers in EMEA, APAC and US.In our role you will work remotely and be part of the sponsor's global
Reference
JR139255
Expiry date
01/01/0001
Author
Author
Salary
Location
Basking Ridge, NJ
Location
Boston
Basking Ridge, NJ
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
What you will be doing Organizes and delivers analyzable reports and metrics to the clinical study leadSchedules and coordinates meetings, prepares agendas, presentation materials and minutes for clin
Reference
JR143385
Expiry date
01/01/0001
Author
Author
Salary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Associate to join our diverse and dynamic team.To be an integral part of the study team by providing administrative and project tracking support to the Proje
Reference
JR143056
Expiry date
01/01/0001
Author
Author
Salary
Location
UK, Reading
Location
Reading
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
Job title - CTA Location - London or surrounding areas (must be able to commit to 2 days in the sponsors office in White City, London)Fully sponsor dedicatedWe are currently seeking a Clinical Trial A
Reference
JR143347
Expiry date
01/01/0001
Author
Author
Salary
Location
China, Beijing
Location
Beijing
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a

Skills Required