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For Companies At a Glance
- Tasks: Join a leading clinical research organisation and manage site visits and compliance.
- Company: World's largest clinical research organisation focused on healthcare intelligence.
- Benefits: Competitive salary, health insurance, flexible benefits, and work-life balance.
- Why this job: Make a real impact in clinical research while travelling and collaborating with diverse teams.
- Qualifications: Bachelor’s in Life Sciences or equivalent, with 2+ years of monitoring experience.
- Other info: Inclusive culture with opportunities for personal and professional growth.
The predicted salary is between 36000 - 60000 £ per year.
What You Will Be Doing
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
- Serve as the primary point of contact between investigational sites and the sponsor
- Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out
- Ensure site compliance with ICH-GCP, SOPs, and regulations
- Maintain up-to-date documentation in CTMS and eTMF systems
- Support and track site staff training and maintain compliance records
- Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting
- Support subject recruitment and retention efforts at the site level
- Oversee drug accountability and ensure proper storage, return, or destruction
- Resolve data queries and drive timely, high-quality data entry
- Document site progress and escalate risks or issues to the clinical team
- Assist in tracking site budgets and ensuring timely site payments (as applicable)
- Collaborating with cross-functional partners including CTAs, LTMs, and CTMs
You are
- A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN
- Eligible to work in United States without visa sponsorship
- A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry
- Experienced across multiple therapeutic areas, including Immunology preferred.
- Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
- A clear communicator, problem-solver, and collaborative team player
- Willing and able to travel up to 50% for on-site monitoring visits across the midwest region, preference given to candidates residing in Chicago, IL or Dallas, TX, to support efficient regional travel
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 maximise 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
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
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, colour, 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.
https://careers.iconplc.com/reasonable-accommodations
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.
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Clinical Research Associate - IMM/Cross TA - Chicago (Field Based) employer: ICON Strategic Solutions
Contact Detail:
ICON Strategic Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate - IMM/Cross TA - Chicago (Field Based)
✨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 the company and its culture. Familiarise yourself with their recent projects and values. This will help you tailor your responses and show that you're genuinely interested in being part of their team.
✨Tip Number 3
Practice your answers to common interview questions, especially those related to clinical research scenarios. Use the STAR method (Situation, Task, Action, Result) to structure your responses and highlight your experience effectively.
✨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 our awesome team at ICON.
We think you need these skills to ace Clinical Research Associate - IMM/Cross TA - Chicago (Field Based)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Clinical Research Associate role. Highlight your on-site monitoring experience and any relevant therapeutic areas you've worked in, especially Immunology.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're passionate about clinical research. Share specific examples of how you've ensured compliance with ICH-GCP and local regulations in your previous roles.
Showcase Your Communication Skills: As a Clinical Research Associate, clear communication is key. In your application, demonstrate your ability to collaborate with cross-functional teams and resolve issues effectively.
Apply Through Our Website: We encourage you to apply directly through our careers website. It’s the best way for us to see your application and get you into the process smoothly. Don’t hesitate – we’re excited to hear from you!
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your Stuff
Make sure you brush up on ICH-GCP guidelines and local regulatory requirements. Being able to discuss these confidently will show that you're not just familiar with the basics, but that you truly understand the standards expected in clinical research.
✨Showcase Your Experience
Prepare specific examples from your previous roles where you've successfully managed site visits or resolved data queries. This will help demonstrate your hands-on experience and problem-solving skills, which are crucial for a Clinical Research Associate.
✨Be Ready to Discuss Collaboration
Since this role involves working with cross-functional partners, think of instances where you've collaborated effectively with others. Highlighting your teamwork skills will show that you can thrive in a collaborative environment.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's culture, team dynamics, and expectations for the role. This not only shows your interest in the position but also helps you gauge if it's the right fit for you.
