At a Glance
- Tasks: Monitor clinical studies and ensure high-quality data collection for real-world evidence.
- Company: Join ICON, a leading healthcare intelligence and clinical research organisation.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
- Other info: Inclusive culture with opportunities for mentorship and career growth.
- Why this job: Make a real impact in clinical research and contribute to patient safety and effectiveness.
- Qualifications: Advanced degree in Life Sciences and experience in clinical research required.
The predicted salary is between 37000 - 45000 £ per year.
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 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) and medical device studies, 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 across both device and IP trials.
- 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 (~6–8 days per month).
- Excellent communication, stakeholder management, and influencing skills.
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 designed to be competitive within each country and 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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.
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.
Clinical Research Associate employer: IRE
ICON is an exceptional employer that prioritises integrity, collaboration, and inclusion, making it a fantastic place for professionals in the healthcare intelligence and clinical research field. With a strong commitment to employee wellbeing, ICON offers a competitive rewards package, comprehensive health programmes, and ample opportunities for career development, all while fostering a diverse and dynamic work culture. Whether working from home or in the office, employees are empowered to manage complex projects and contribute meaningfully to advancing patient-centric outcomes.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching ICON and understanding their late phase studies. Be ready to discuss how your experience aligns with their mission and values. Show them you’re not just another candidate, but someone who genuinely wants to contribute to their success.
✨Tip Number 3
Practice your answers to common CRA interview questions. Think about your past experiences and how they relate to site monitoring, data integrity, and stakeholder engagement. The more prepared you are, the more confident you'll feel during the interview.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining the ICON team and ready to make an impact in clinical research.
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience in late phase studies and any relevant skills that match the job description. We want to see how you can contribute to our mission!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background aligns with our values at ICON. Let us know what excites you about this opportunity!
Showcase Your Skills:Don’t forget to highlight your expertise in site monitoring, data integrity, and regulatory requirements. We’re looking for someone who can manage multiple sites effectively, so make sure we see that in your application!
Apply Through Our Website:We encourage you to apply directly through our careers site. It’s the best way to ensure your application gets to the right people. Plus, you’ll find more info about the benefits we offer and our inclusive culture!
How to prepare for a job interview at IRE
✨Know Your Stuff
Make sure you brush up on your knowledge of ICH-GCP and regulatory requirements. Being able to discuss these in detail will show that you’re not just familiar with the basics, but that you truly understand the nuances of late phase studies.
✨Showcase Your Experience
Prepare specific examples from your past roles where you successfully managed site monitoring or resolved issues. Highlighting your hands-on experience with both investigational products and medical devices will set you apart from other candidates.
✨Engage with Stakeholders
Think about how you’ve built relationships with investigators and site staff in the past. Be ready to share strategies you’ve used to foster collaboration and engagement, as this is crucial for successful study execution.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to late phase studies and their expectations for the role. This shows your genuine interest in the position and helps you assess if it’s the right fit for you.
