At a Glance
- Tasks: Lead clinical trial monitoring and ensure adherence to protocols and regulations.
- Company: Join ICON, 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: Make a real impact in clinical research 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.
SSU CRAICON 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.
Location - 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:You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:
- 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.
You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:- 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%).
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, 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.
Clinical Research Associate - reduced travel employer: IRE
At ICON, we pride ourselves on being a world-leading healthcare intelligence and clinical research organisation that champions innovation and excellence. Our inclusive work culture fosters collaboration and personal growth, offering competitive benefits such as flexible working arrangements, comprehensive health insurance, and a global employee assistance programme. Join us in the UK to contribute to meaningful clinical development while enjoying a supportive environment that values your well-being and professional advancement.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate - reduced travel
✨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 a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their mission and values, especially around innovation and inclusivity, so you can show how you align with their goals during the chat.
✨Tip Number 3
Practice your responses to common interview questions, but keep it natural. Use the STAR method (Situation, Task, Action, Result) to structure your answers, especially when discussing your experience in clinical trial monitoring.
✨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
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the job description. Highlight your clinical trial monitoring experience and any relevant qualifications to show us you're the right fit!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're interested in the role and how your background aligns with our mission at ICON. Keep it concise but impactful!
Showcase Your Soft Skills:We value communication and interpersonal skills just as much as technical expertise. Be sure to mention any experiences where you've successfully collaborated with teams or built relationships with stakeholders.
Apply Through Our Website:We encourage you to apply directly through our careers site. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity!
How to prepare for a job interview at IRE
✨Know Your Stuff
Make sure you brush up on your clinical trial knowledge, especially around monitoring practices and GCP standards. Familiarise yourself with the specific protocols and regulations relevant to the role, as this will show your commitment and expertise.
✨Showcase Your Experience
Prepare to discuss your previous experience in clinical research, particularly any SSV and submission work you've done. Be ready to share specific examples of how you've managed multiple sites or resolved issues during trials, as this will highlight your problem-solving skills.
✨Build Rapport
During the interview, focus on demonstrating your interpersonal skills. Talk about how you've built relationships with site personnel and stakeholders in the past. This is crucial for a role that requires collaboration and effective communication.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's culture, the team you'll be working with, and the specific challenges they face in clinical trials. This not only shows your interest but also helps you gauge if the company is the right fit for you.
