At a Glance
- Tasks: Conduct clinical trials and ensure compliance with protocols while managing study sites.
- Company: Join ICON, a global leader in clinical research with a supportive culture.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
- Other info: Opportunities for travel and career growth in a dynamic environment.
- Why this job: Make a real impact in healthcare by contributing to innovative clinical research.
- Qualifications: 12 months of monitoring experience and knowledge of clinical trials required.
The predicted salary is between 36000 - 60000 £ per year.
Icon plc is a world‑leading healthcare intelligence and clinical research organization. You’re invited to join us on our mission to shape the future of clinical development.
Job title
CRA (must have at least 12 months’ monitoring experience)
Location
Must be based in the UK
Fully sponsor dedicated
Role Overview
Working fully embedded within a growing program as a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key Responsibilities
- Conducting site qualification, initiation, monitoring, and close‑out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolving queries to maintain high‑quality clinical data.
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
Your Profile
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required Qualifications And Experience
- Bachelor’s degree in a scientific or healthcare‑related field.
- Minimum of 12 months experience as a Clinical Research Associate.
- Must have experience working on Oncology trials.
- In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines.
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast‑paced environment.
- Willingness to travel as required (approximately 60 %)
What ICON Can Offer You
In addition to your competitive salary, ICON offers a range of additional benefits focused on well‑being and work‑life balance.
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 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 a request here.
Clinical Research Associate - 12 months' monitoring experience required in Reading employer: ICON Strategic Solutions
ICON Strategic Solutions is an exceptional employer, offering a dynamic work environment that prioritises employee well-being and professional growth. With comprehensive benefits including health insurance, flexible leave options, and a commitment to inclusivity, ICON fosters a culture of collaboration and support, making it an ideal place for Clinical Research Associates looking to advance their careers while contributing to meaningful clinical research across the UK.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate - 12 months' monitoring experience required in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. 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 researching ICON and understanding their values and projects. Tailor your responses to show how your 12 months of monitoring experience aligns with their needs. Confidence is key, so practice common interview questions with a friend!
✨Tip Number 3
Don’t just apply—follow up! After submitting your application through our website, send a polite email to express your enthusiasm for the role. It shows initiative and keeps you on their radar.
✨Tip Number 4
Stay organised! Keep track of the jobs you’ve applied for, the contacts you’ve made, and any follow-up actions. This will help you stay focused and ensure you don’t miss any opportunities that come your way.
We think you need these skills to ace Clinical Research Associate - 12 months' monitoring experience required in Reading
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your 12 months of monitoring experience. We want to see how your skills align with the role, so don’t be shy about showcasing relevant projects or responsibilities!
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 us at ICON. Keep it engaging and personal!
Showcase Your Knowledge:In your application, demonstrate your understanding of GCP/ICH guidelines and the drug development process. We love candidates who can speak our language and show they’re up to date with industry standards.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your Monitoring Experience
Make sure you can clearly articulate your 12 months of monitoring experience. Be ready to discuss specific trials you've worked on, the challenges you faced, and how you overcame them. This will show that you have the practical knowledge needed for the role.
✨Familiarise Yourself with GCP/ICH Guidelines
Brush up on Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines. Being able to reference these standards during your interview will demonstrate your understanding of compliance and regulatory requirements, which is crucial for a Clinical Research Associate.
✨Prepare Questions About Site Management
Think of insightful questions regarding site management and collaboration. Asking about how ICON supports its CRAs in managing study sites or how they handle data integrity issues shows your genuine interest in the role and your proactive approach to problem-solving.
✨Showcase Your Travel Flexibility
Since the role requires significant travel, be prepared to discuss your availability and willingness to travel. Highlight any previous experiences where you successfully managed travel logistics while maintaining productivity, as this will reassure them of your adaptability.
