At a Glance
- Tasks: Oversee clinical trials, ensuring compliance and data integrity while supporting site staff.
- Company: Join ICON plc, a leading healthcare intelligence and clinical research organisation.
- Benefits: Competitive salary, health insurance, flexible benefits, and global support programmes.
- Why this job: Make a real impact in oncology research while working in a diverse and inclusive environment.
- Qualifications: 3+ years as a CRA with oncology experience and strong organisational skills.
- Other info: Opportunities for travel and career growth in a dynamic team.
The predicted salary is between 36000 - 60000 £ 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 (3+ years), 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.
- Ability to travel at least 60% of the time (international and domestic – fly and drive) and should possess a valid driver's license.
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.
- 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.
At ICON, inclusion and 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.
CRA UK - Oncology experience required in London employer: ICON
Contact Detail:
ICON Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CRA UK - Oncology experience required in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the oncology field and let them know you're on the lookout for CRA roles. 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 brushing up on your oncology knowledge and clinical trial processes. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.
✨Tip Number 3
Showcase your experience! When you get the chance to chat with potential employers, highlight your previous oncology projects and how you've contributed to successful trials. Real-life examples can make a huge impact.
✨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 genuinely interested in joining our team at ICON.
We think you need these skills to ace CRA UK - Oncology experience required in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your oncology experience and relevant skills. We want to see how your background aligns with the CRA role, so don’t be shy about showcasing your achievements!
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 experience makes you a perfect fit for our team at ICON. Keep it engaging and personal.
Showcase Your Soft Skills: As a CRA, communication and relationship-building are key. Make sure to highlight your interpersonal skills and any experiences where you’ve successfully collaborated with teams or managed stakeholders.
Apply Through Our Website: We encourage you to apply directly through our careers site. It’s the best way to ensure your application gets the attention it deserves. Plus, you’ll find all the info about the role and our awesome benefits there!
How to prepare for a job interview at ICON
✨Know Your Oncology Stuff
Make sure you brush up on your oncology knowledge before the interview. Familiarise yourself with the latest trends, treatments, and clinical trial processes in oncology. This will not only show your expertise but also demonstrate your genuine interest in the field.
✨Showcase Your Experience
Prepare to discuss your previous experiences as a Clinical Research Associate. Highlight specific projects you've worked on, particularly those involving oncology. Use the STAR method (Situation, Task, Action, Result) to structure your answers and make them impactful.
✨Demonstrate Problem-Solving Skills
Be ready to share examples of challenges you've faced in clinical trials and how you resolved them. ICON values strong problem-solving abilities, so think of situations where you had to think on your feet or adapt quickly to changes.
✨Build Rapport with Interviewers
During the interview, focus on building a connection with your interviewers. Ask insightful questions about their experiences at ICON and express your enthusiasm for joining their team. A positive attitude and good communication skills can set you apart from other candidates.