Clinical Research Associate
- Reading
- Clinical Monitoring
- ICON Full Service & Corporate Support
- Remote or Office
Senior Talent Acquisition Business Partner
- Full Service Division
About the role
CRA II Late Phase
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.
CRA II (will consider Senior CRA) Late Phase
Home based in the UK
We are seeking a Clinical Research Associate to join ICON Commercialisation & Outcomes (ICO) — our Late Phase business. This is an exciting opportunity to work on post-marketing, real-world, and late phase studies, supporting evidence generation that demonstrates value, safety, and effectiveness in broader patient populations.
As a CRA in our Late Phase team, you will play a critical role in ensuring high-quality delivery across a mix of interventional (IP), observational and medical device studies, in various therapeutic indications, contributing to successful outcomes that shape clinical and commercial strategy.
Key Responsibilities
- Site Monitoring & Oversight
Conduct on-site and remote monitoring visits across late phase studies, ensuring compliance with protocols, ICH-GCP, regulatory requirements, and applicable device regulations. - Late Phase Study Delivery
Support execution of post-authorisation, observational, and interventional studies, ensuring high-quality data collection and real-world evidence generation. - Site Performance & Issue Resolution
Evaluate site performance, identify risks, and implement solutions to ensure studies are delivered on time and to quality standards. - Cross-Functional Collaboration
Partner with project teams, medical, data management, and commercial stakeholders to ensure efficient study delivery and reporting. - Training & Mentorship
Provide guidance and support to site personnel and junior CRAs, maintaining consistency and best practice, where applicable. - Stakeholder Engagement
Build strong relationships with investigators and site staff to drive engagement and successful study execution.
Your Profile
- Advanced degree in Life Sciences, Nursing, Pharmacy, or Medicine
- Significant experience as a Clinical Research Associate, ideally within late phase / Phase IV / real-world studies
- Experience across both investigational product (IP) and medical device trials is highly desirable
- Strong understanding of ICH-GCP, regulatory requirements, and post-marketing study environments
- Proven ability to manage multiple sites and competing priorities
- Expertise in site monitoring, data integrity, and risk-based monitoring approaches
- Proficiency in clinical systems (e.g., CTMS, EDC)
- Willingness to travel across the UK to perform on-site visits
- Excellent communication, stakeholder management, and influencing skills
#LI-SB2
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 careers site 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 here
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 here to apply
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
A Day In The LifeContent type
BlogsPublish date
04/05/2023
Summary
Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfil
by
Suzaita Hipolito
Teaser label
Career ProgressionContent type
BlogsPublish date
03/20/2020
Summary
Navigating the world of graduate schemes and positions can be daunting, especially if you’re not quite sure of the role or company you want to align yourself with. At ICON, we recognise what a s
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