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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, flexible benefits, health insurance, and a supportive work-life balance.
- Why this job: Be part of a diverse team shaping the future of clinical development with impactful work.
- Qualifications: Bachelor's degree in a scientific field and 2 years of relevant experience required.
- Other info: We encourage all applicants to apply, regardless of meeting every requirement.
The predicted salary is between 28800 - 43200 £ per year.
Senior CRA – multi sponsor
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 Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON, 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.
This position is working for our full service team so is multi therapy and multi sponsor.
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, (at least 3 years) with a strong understanding of clinical trial processes and regulatory requirements.
- Oncology/Hematology experience is preferred
- 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.
#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 #J-18808-Ljbffr
CRA II employer: ICON plc
Contact Detail:
ICON plc 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 can provide valuable insights into the company culture and expectations, which can be beneficial during your application process.
✨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 your enthusiasm for the role by researching ICON's recent projects and contributions to clinical development. Mentioning these in your discussions can demonstrate your genuine interest in being part of their mission.
We think you need these skills to ace CRA II
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the Clinical Research Associate II position. Tailor your application to highlight relevant experiences that align with these expectations.
Highlight Relevant Experience: In your CV and cover letter, emphasise your experience as a Clinical Research Associate, particularly any specific projects or trials you have worked on. Mention your familiarity with clinical trial processes, regulations, and ICH-GCP guidelines.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for clinical research and how you can contribute to ICON's mission. Use specific examples to demonstrate your skills and achievements.
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 plc
✨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 past roles. This will highlight your ability to facilitate smooth study conduct.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving abilities. Think about challenges you've faced in previous trials and how you resolved them. This will show your critical thinking and adaptability in a fast-paced environment.
✨Express Your Passion for Innovation
ICON values innovation and excellence. Be ready to discuss why you're passionate about clinical research and how you can contribute to advancing innovative treatments and therapies. This will align your personal goals with the company's mission.
