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- Tasks: Oversee clinical trials, ensuring compliance and data integrity while supporting site staff.
- 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 global employee assistance programme.
- Why this job: Join a diverse team shaping the future of clinical development with a focus on inclusion and excellence.
- Qualifications: Advanced degree in life sciences or related field; extensive CRA experience required.
- Other info: We encourage all applicants to apply, even if you don't meet every requirement.
The predicted salary is between 28800 - 48000 £ per year.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
What You Will Be Doing:
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile:
- Advanced degree in a relevant field such as life sciences, nursing, or medicine.
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
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, 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, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We’re proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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.
Senior CRA employer: ICON plc
Contact Detail:
ICON plc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior CRA
✨Tip Number 1
Familiarise yourself with the latest Good Clinical Practice (GCP) guidelines and regulatory requirements. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high standards in clinical trials.
✨Tip Number 2
Network with current or former employees of ICON plc on platforms like LinkedIn. Engaging with them can provide valuable insights into the company culture and expectations, which can be beneficial during your interview.
✨Tip Number 3
Prepare specific examples from your past experience that showcase your ability to manage multiple sites and projects. Highlighting your problem-solving skills and how you've ensured data integrity will resonate well with the hiring team.
✨Tip Number 4
Research ICON's recent clinical trials and their impact on healthcare. Being knowledgeable about their work will allow you to ask informed questions during the interview, showing your genuine interest in the role and the company.
We think you need these skills to ace Senior CRA
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Senior CRA position at ICON plc. Understand the key responsibilities and required qualifications to tailor your application accordingly.
Highlight Relevant Experience: In your CV and cover letter, emphasise your extensive experience as a Clinical Research Associate. Include specific examples of how you've managed clinical trials, ensured data integrity, and adhered to regulatory requirements.
Showcase Soft Skills: ICON values excellent communication and interpersonal skills. Make sure to highlight your ability to build relationships with site personnel and stakeholders, as well as your problem-solving capabilities in your application.
Tailor Your Application: Customise your CV and cover letter to reflect the values and culture of ICON plc. Mention your commitment to diversity and inclusion, and how you can contribute to their mission of shaping the future of clinical development.
How to prepare for a job interview at ICON plc
✨Understand the Role Thoroughly
Before your interview, make sure you have a solid understanding of the Senior CRA role. Familiarise yourself with clinical trial processes, regulatory requirements, and Good Clinical Practice (GCP) standards. This will help you answer questions confidently and demonstrate your expertise.
✨Prepare for Scenario-Based Questions
Expect to be asked about specific scenarios you might encounter as a Senior CRA. Prepare examples from your past experience where you successfully managed site performance or resolved issues. This will showcase your problem-solving skills and ability to handle challenges.
✨Highlight Your Communication Skills
As a Senior CRA, strong communication and interpersonal skills are crucial. Be ready to discuss how you've built effective relationships with site personnel and stakeholders in previous roles. Use examples that illustrate your ability to influence and drive compliance.
✨Showcase Your Organisational Skills
The role requires managing multiple sites and projects simultaneously. Be prepared to discuss your organisational strategies and tools you use to keep track of various tasks. This will demonstrate your capability to handle the demands of the position effectively.
