At a Glance
- Tasks: Lead clinical trial monitoring and ensure adherence to protocols and regulations.
- Company: Join ICON plc, a leading healthcare intelligence and clinical research organisation.
- Benefits: Competitive salary, health insurance, flexible benefits, and global support programmes.
- Other info: Opportunity for career growth with reduced travel and a focus on work-life balance.
- Why this job: Shape the future of clinical development while enjoying a supportive and inclusive culture.
- Qualifications: Bachelor's degree in a relevant field and extensive CRA experience required.
The predicted salary is between 35000 - 45000 € per year.
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.
Must be based in the UK. Fully sponsor dedicated. We're looking for individuals that are interested in a short term assignment as a SSU CRA who're happy to transition into a standard CRA once the SSU assignment comes to an end.
What You Will Do:
- Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
- Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile:
- Strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
- Bachelor's degree in a relevant scientific discipline or healthcare-related field.
- Must have SSV and submission experience.
- 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.
- Willingness to travel as required (approximately 60%).
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 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 & 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 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.
Clinical Research Associate - reduced travel in Reading employer: ICON
At ICON plc, we pride ourselves on being a world-leading healthcare intelligence and clinical research organisation that champions innovation and excellence. Our inclusive work culture fosters employee growth through diverse opportunities and competitive benefits, including comprehensive health insurance, flexible leave entitlements, and a strong focus on work-life balance. Join us in the UK as a Clinical Research Associate and be part of a team dedicated to shaping the future of clinical development while enjoying a supportive environment that values your contributions.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate - reduced travel in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical trial processes and regulatory requirements. 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 skills! During interviews, highlight your experience in monitoring practices and site management. Use specific examples to demonstrate how you've tackled challenges in past roles – this will make you stand out.
✨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 Clinical Research Associate - reduced travel in Reading
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight your relevant experience, especially in clinical trial monitoring and any specific skills that match the job description. We want to see how you fit into our mission!
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 background makes you a great fit for the role. Don’t forget to mention your willingness to transition into a standard CRA position!
Showcase Your Skills:In your application, be sure to showcase your organisational and problem-solving skills. Mention any experience you have with site management and data integrity, as these are key for us at ICON. We love seeing candidates who can manage multiple projects effectively!
Apply Through Our Website:We encourage you to apply through our careers site. It’s the best way to ensure your application gets the attention it deserves. Plus, you’ll find more info about the benefits we offer and our inclusive culture!
How to prepare for a job interview at ICON
✨Know Your Stuff
Make sure you brush up on your clinical trial knowledge, especially around monitoring practices and regulatory requirements. Familiarise yourself with Good Clinical Practice (GCP) standards, as you'll likely be asked about them during the interview.
✨Showcase Your Experience
Prepare to discuss your previous roles as a Clinical Research Associate. Highlight specific examples where you've successfully managed multiple sites or resolved issues during trials. This will demonstrate your ability to handle the responsibilities of the role.
✨Build Rapport
Since relationship-building is key in this role, practice how you would engage with site personnel and stakeholders. Think of ways to convey your interpersonal skills and how you can influence compliance within a complex environment.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's culture, the team you'll be working with, and the specifics of the SSU CRA role. This shows your genuine interest in the position and helps you assess if it's the right fit for you.
