CRA II

CRA II

Reading Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join us as a Clinical Research Associate II, conducting and monitoring clinical trials.
  • Company: ICON plc is a leading healthcare intelligence and clinical research organisation committed to innovation.
  • Benefits: Enjoy competitive salary, flexible benefits, health insurance, and work-life balance perks.
  • Why this job: Be part of a diverse team shaping the future of clinical development with impactful work.
  • Qualifications: Bachelor's degree in a scientific field and 2 years of CRA experience required.
  • Other info: We value inclusion and encourage all qualified candidates to apply, regardless of background.

The predicted salary is between 36000 - 60000 £ 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. We are currently seeking a Clinical Research Associate II for our full-service team in the UK. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing:

  • 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 resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Your profile:

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • 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.
  • Ability to travel across the UK as required.
  • Fluent in English.

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 focus on well-being and work-life balance opportunities for you and your family. Our benefits include:

  • Various annual leave entitlements
  • A range of health insurance options 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 professionals who support your 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 regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. If you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position due to a medical condition or disability, please let us know or submit a request.

If you’re interested in the role but unsure if you meet all requirements, we encourage you to apply. You might be exactly what we’re looking for at ICON, whether for this or other roles.

CRA II employer: ICON plc

At ICON plc, we pride ourselves on being a world-leading healthcare intelligence and clinical research organisation that values innovation and excellence. Our inclusive work culture fosters collaboration and personal growth, offering competitive benefits such as flexible annual leave, comprehensive health insurance, and a global employee assistance programme. Join us in the UK as a Clinical Research Associate II, where you will have the opportunity to contribute to groundbreaking clinical trials while enjoying a supportive environment that prioritises your well-being and professional development.
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Contact Detail:

ICON plc Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land CRA II

✨Tip Number 1

Familiarise yourself with the latest ICH-GCP guidelines and clinical trial regulations. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high standards in clinical research.

✨Tip Number 2

Network with professionals in the clinical research field, especially those who work at ICON or similar organisations. Attend industry conferences or webinars to make connections and learn more about the company culture and expectations.

✨Tip Number 3

Prepare for potential interview questions by reviewing common scenarios faced by Clinical Research Associates. Think of examples from your past experience that showcase your problem-solving skills and ability to ensure protocol compliance.

✨Tip Number 4

Showcase your organisational and communication skills during the interview process. Be ready to discuss how you manage multiple tasks and collaborate with site staff to ensure smooth study conduct, as these are key aspects of the CRA II role.

We think you need these skills to ace CRA II

Clinical Trial Management
Knowledge of ICH-GCP Guidelines
Data Integrity Assurance
Site Monitoring and Management
Protocol Compliance
Medical Data Interpretation
Strong Communication Skills
Organisational Skills
Attention to Detail
Problem-Solving Skills
Collaboration with Investigators
Data Review and Query Resolution
Ability to Work Independently
Adaptability in Fast-Paced Environments
Travel Flexibility across the UK

Some tips for your application 🫡

Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the Clinical Research Associate II position. Tailor your application to highlight relevant experiences that align with these expectations.

Highlight Relevant Experience: In your CV and cover letter, emphasise your previous experience as a Clinical Research Associate, particularly any specific projects or trials you have worked on. Use quantifiable achievements to demonstrate your impact in previous roles.

Showcase Your Skills: Make sure to showcase your organisational and communication skills in your application. Provide examples of how you've successfully collaborated with teams or managed multiple tasks in a fast-paced environment.

Craft a Compelling Cover Letter: Write a personalised cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role and the company. Mention why you are drawn to ICON plc and how you can contribute to their mission.

How to prepare for a job interview at ICON plc

✨Know Your Clinical Trial Processes

Make sure you have a solid understanding of clinical trial processes, regulations, and ICH-GCP guidelines. Be prepared to discuss your experience in these areas and how you've applied this knowledge in previous roles.

✨Showcase Your Communication Skills

As a CRA II, you'll need to collaborate with investigators and site staff. Highlight your communication skills during the interview by providing examples of how you've effectively worked with teams or resolved conflicts in past projects.

✨Demonstrate Attention to Detail

Attention to detail is crucial in clinical research. Prepare to discuss specific instances where your attention to detail has positively impacted data integrity or patient safety in your previous work.

✨Be Ready to Discuss Travel Flexibility

Since the role requires travel across the UK, be prepared to talk about your availability and willingness to travel. Share any relevant experiences that demonstrate your adaptability and commitment to meeting project needs.

CRA II
ICON plc
Location: Reading
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