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- Tasks: Join us as a Clinical Research Associate II, conducting and monitoring clinical trials.
- Company: ICON plc is a leading healthcare intelligence and clinical research organisation committed to innovation.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and a supportive work-life balance.
- Why this job: Make a real impact in healthcare while working in an inclusive and dynamic environment.
- Qualifications: Bachelor's degree in a scientific field and 2 years of CRA experience required.
- Other info: We encourage all applicants to apply, regardless of meeting every requirement.
The predicted salary is between 28800 - 43200 £ per year.
CRA II 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 Clinical Research Associate II for our full service team in the UK. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports. Your profile Bachelor\’s degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Ability to travel across the UK as required. Fluent in English. 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. 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 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. #J-18808-Ljbffr
CRA II employer: ICON
Contact Detail:
ICON Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CRA II
✨Tip Number 1
Familiarise yourself with the latest ICH-GCP guidelines and clinical trial processes. This knowledge will not only help you during interviews but also demonstrate your commitment to maintaining high standards in clinical research.
✨Tip Number 2
Network with current or former Clinical Research Associates at ICON or similar organisations. Engaging in conversations about their experiences can provide valuable insights into the role and the company culture, which you can reference in your discussions.
✨Tip Number 3
Prepare to discuss specific examples from your previous experience that highlight your organisational and communication skills. Being able to articulate how you've successfully managed trials or resolved data queries will set you apart.
✨Tip Number 4
Show enthusiasm for the mission of ICON and the impact of clinical research on patient care. Expressing a genuine interest in contributing to innovative treatments can resonate well with interviewers and align with the company's values.
We think you need these skills to ace CRA II
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Clinical Research Associate II at ICON. Familiarise yourself with the key tasks such as conducting site visits, ensuring protocol compliance, and collaborating with site staff.
Tailor Your CV: Highlight your relevant experience in clinical research, particularly any roles that involved monitoring or managing clinical trials. Emphasise your knowledge of ICH-GCP guidelines and any specific achievements that demonstrate your organisational and communication skills.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for clinical research and your alignment with ICON's mission. Mention how your background can contribute to their goal of advancing innovative treatments.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial in the role of a Clinical Research Associate.
How to prepare for a job interview at ICON
✨Know Your Clinical Trial Processes
Make sure you have a solid understanding of clinical trial processes, regulations, and ICH-GCP guidelines. Brush up on your knowledge before the interview, as this will demonstrate your expertise and commitment to the role.
✨Showcase Your Communication Skills
As a Clinical Research Associate II, you'll need strong communication skills. Prepare examples of how you've effectively collaborated with investigators and site staff in the past, highlighting your ability to facilitate smooth study conduct.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving abilities. Think about past experiences where you had to resolve data queries or ensure protocol compliance, and be ready to discuss these situations in detail.
✨Emphasise Your Attention to Detail
Attention to detail is crucial in clinical research. Be prepared to discuss how you maintain high-quality clinical data and ensure patient safety throughout the trial process. Specific examples will help illustrate your capabilities.
