At a Glance
- Tasks: Monitor clinical trials and ensure high-quality outcomes while collaborating with your team.
- Company: Join ICON, a leading healthcare intelligence and clinical research organisation.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
- Other info: Inclusive culture with opportunities for career growth and personal development.
- Why this job: Make a real impact in clinical development and enhance patient safety.
- Qualifications: Degree in medicine or science, with clinical trial monitoring experience.
The predicted salary is between 30000 - 40000 £ 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.
As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.
What You Will Do:
Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders. Key responsibilities include:
- Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.
- Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
- Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
- Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.
Your Profile:
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
- University degree in medicine, science, or equivalent.
- Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data.
- Excellent written and verbal communication in English.
- Good social skills enabling you to deal with queries in a timely manner.
- 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. 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.
Cra I employer: IRE
Contact Detail:
IRE Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Cra I
✨Tip Number 1
Network like a pro! Reach out to current or former employees at ICON through LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by knowing your stuff! Research ICON’s recent projects and their approach to clinical trials. This shows you're genuinely interested and ready to contribute to their mission.
✨Tip Number 3
Practice your answers to common interview questions. Think about how your experience aligns with the CRA I role and be ready to share specific examples of your past work 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 serious about joining the ICON team.
We think you need these skills to ace Cra I
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the CRA I role. Highlight your relevant clinical trial monitoring experience and any specific skills that match the job description. We want to see how you fit into our mission at ICON!
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 aligns with our values at ICON. Keep it engaging and personal – we love to see your personality!
Showcase Your Communication Skills: Since excellent written communication is key for this role, make sure your application is clear and concise. Avoid jargon and keep it professional yet approachable. We appreciate good social skills, so let that shine through!
Apply Through Our Website: We encourage you to apply directly through our careers site. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you can explore more about what we offer at ICON while you’re there!
How to prepare for a job interview at IRE
✨Know Your ICH-GCP Guidelines
Make sure you brush up on the ICH-GCP guidelines before your interview. Being able to discuss these in detail will show that you understand the regulatory framework and can ensure compliance, which is crucial for a CRA I role.
✨Showcase Your Communication Skills
Since excellent written and verbal communication is key, prepare examples of how you've effectively communicated with stakeholders in past roles. This could be through reports, presentations, or even resolving queries – make it relatable!
✨Demonstrate Your Team Spirit
ICON values collaboration, so think of instances where you've worked closely with a team to achieve a goal. Highlight how you contributed to maintaining strong relationships with colleagues and site staff, as this will resonate well with their culture.
✨Prepare for Travel Questions
With the role requiring approximately 60% travel, be ready to discuss your flexibility and willingness to travel. Share any previous experiences where travel was involved and how you managed your time effectively while on the go.