IHCRA
Talent Acquisition Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please click here to view live vacancies.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
ICONs Clinical Operations team is actively looking to hire a significant number of In-house CRAs. You will be part of our world class development program which fast tracks your growth into a traveling CRA within 4-6 months. If you enjoy travel, are ready for your next step in your clinical research career, and are passionate about ICONs mission to bring life-saving therapies to market, this is your chance to join the team!
ICON's award-winning study execution capabilities have led to the approval of 18 of the world's top 20 best-selling drugs. As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them? Apply Now.
The Role
Become familiar with ICON's SOPs/WPs, ICH GCP guidelines, appropriate regulations, ICON systems and the principles of and assist with investigator recruitment
Maintain timelines and ensure accuracy and completeness of data entered into ICON systems
Serve as the primary in-house contact for sites and investigators participating in studies
Conduct and completes remote site management activities, with support as needed, according to applicable SOPS and the Study Monitoring Plan.
To contact Clinical sites for specific requests (e.g. enrolment updates, missing documentation, data entry timeliness, data query follow-up, CDA finding follow-up, and action Item resolution or other sponsor specific CRA tasks.
Take responsibility for project tasks and sees these tasks through to successful completion, with support.
Maintain a professional interpersonal relationship with study team, sites, and Sponsors
Participate in QA Audits as needed.
Regularly attend and gives to project specific and departmental meetings
Ability and willingness to travel as needed (drive and fly)
Maintain Sponsor and patient confidentiality
Other duties as assigned
What you need
Minimum Bachelor's degree in a life science
At least 12 months of a CTA/Clinical Trial Assistant or similar role experience within the clinical/pharmaceutical industry
Understanding of ICH GCP Compliance
Excellent communication and organizational skills
A phenomenal teammate
Benefits of Working at ICON
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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 through the form below.
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
Our PeopleContent type
BlogsPublish date
01/26/2026
Summary
Sometimes the best way to recognise what you have is to experience life without it. For Izabella Grimaldi, a Clinical Research Associate II based in Brazil, that realisation came after seven months wo
Teaser label
IndustryContent type
BlogsPublish date
01/20/2026
Summary
Understanding the Difference Between CRA, CTA, and SMA Clinical research job titles can be confusing, particularly for those new to the industry. Acronyms such as CRA, CTA and SMA appear frequentl
Teaser label
Inside ICONContent type
BlogsPublish date
01/05/2026
Summary
Interviewing at ICON: What to Expect Applying for a new role can feel uncertain, particularly when recruitment processes use digital tools or assessments that may be unfamiliar. At ICON, we want ca
Similar jobs at ICON
Salary
Location
UK, Swansea
Location
Dublin
Reading
Swansea
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Data Scientist Lead
Job Type
Permanent
Description
We are currently seeking a Lead Clinical Data Science Programmer to join our diverse and dynamic team. As a Lead Clinical Data Science Programmer at ICON, you will play a key role in designing and dev
Reference
JR136487
Expiry date
01/01/0001
Author
Rowena DeswertAuthor
Rowena DeswertSalary
Location
Turkey, Ankara
Location
Ankara
Remote Working
Office or Home
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
JR143140
Expiry date
01/01/0001
Author
Tuba SuAuthor
Tuba SuSalary
Location
UK, Swansea
Location
Dublin
Reading
Swansea
Belfast
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Technical Project Management
Non-Clinical Project Management
Job Type
Permanent
Description
We are currently seeking a Principal Clinical System Lead to join our diverse and dynamic team. As a Principal Clinical System Lead at ICON, you will play a pivotal role in providing strategic leaders
Reference
JR137205
Expiry date
01/01/0001
Author
Rowena DeswertAuthor
Rowena DeswertSalary
Location
UK, Swansea
Location
Johannesburg
Swansea
Belfast
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Systems
Job Type
Permanent
Description
We are currently seeking a Manager, Clinical Systems to join our diverse and dynamic team. As a Manager, Clinical Systems at ICON, you will play a pivotal role in overseeing the implementation and mai
Reference
JR141197
Expiry date
01/01/0001
Author
Rowena DeswertAuthor
Rowena DeswertSalary
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
Dariusz SternlichtAuthor
Dariusz SternlichtSalary
Location
India, Bangalore
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Bangalore
Bengaluru
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Medical Writing
Job Type
Permanent
Description
We are currently seeking an Analytical Writer to join our diverse and dynamic team. As an Analytical Writer, you will play a key role in supporting bioanalytical and clinical research activities throu
Reference
JR141947
Expiry date
01/01/0001
Author
Kashifa TahseenAuthor
Kashifa Tahseen