Amgen FSP Clinical Research Associate in Reading
Amgen FSP Clinical Research Associate

Amgen FSP Clinical Research Associate in Reading

Reading Full-Time 36000 - 60000 ÂŁ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Design and analyse clinical trials, ensuring patient safety and data integrity.
  • Company: Join ICON plc, a leading healthcare intelligence and clinical research organisation.
  • Benefits: Competitive salary, health insurance, flexible benefits, and work-life balance.
  • Why this job: Make a real impact in advancing innovative treatments while working with a diverse team.
  • Qualifications: Bachelor's degree in a scientific field and 2 years of CRA experience required.
  • Other info: Inclusive culture with opportunities for career growth and development.

The predicted salary is between 36000 - 60000 ÂŁ 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 home-based Clinical Research Associate II or SCRA to join our diverse and dynamic team. This is single‑sponsor dedicated – and you’ll be joining an existing team of experienced CRAs already well‑versed in the program requirements. There is the requirement to attend one remote interview only with the internal Hiring Manager.

As a Clinical Research Associate 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.

Typical 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 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 at least 50% of the time and should possess a valid driver’s license.
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, 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 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.

Amgen FSP Clinical Research Associate 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 collaboration and personal growth, offering competitive benefits such as flexible working arrangements, comprehensive health insurance, and a global employee assistance programme to support your well-being. Join us in shaping the future of clinical development while enjoying a rewarding career with ample opportunities for professional advancement.
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Contact Detail:

ICON Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Amgen FSP Clinical Research Associate in Reading

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field, especially those who work at ICON or similar companies. A friendly chat can lead to insider info about job openings and even referrals.

✨Tip Number 2

Prepare for that remote interview! Research common questions for Clinical Research Associates and practice your answers. We want you to shine and show off your knowledge of clinical trial processes and regulations.

✨Tip Number 3

Show your passion for patient safety and data integrity during interviews. Share examples from your experience that highlight your attention to detail and commitment to high-quality clinical data. This will resonate well with the hiring team.

✨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 our diverse and dynamic team at ICON.

We think you need these skills to ace Amgen FSP Clinical Research Associate in Reading

Clinical Trial Processes
ICH-GCP Guidelines
Data Integrity
Protocol Compliance
Site Monitoring
Communication Skills
Organisational Skills
Attention to Detail
Data Review
Problem-Solving Skills
Collaboration
Independent Working
Adaptability
Travel Flexibility

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 trials and any specific skills that match the job description. We want to see how you fit into our team!

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 ICON. Keep it concise but impactful – we love a good story!

Showcase Your Skills: Don’t forget to showcase your organisational and communication skills in your application. Mention specific examples where you've demonstrated these abilities in past roles. We’re looking for detail-oriented individuals who can thrive in a fast-paced environment!

Apply Through Our Website: We encourage you to apply through our careers site. It’s the best way to ensure your application gets to us directly. Plus, you’ll find all the info you need about the role and our awesome benefits!

How to prepare for a job interview at ICON

✨Know Your Stuff

Make sure you brush up on your knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Being able to discuss these topics confidently will show the hiring manager that you're well-prepared and serious about the role.

✨Showcase Your Experience

Prepare specific examples from your past work as a Clinical Research Associate. Highlight your experience in site qualification, monitoring, and data integrity. This will help demonstrate your ability to contribute effectively to their team.

✨Ask Smart Questions

Come prepared with insightful questions about the company culture, team dynamics, and the specific projects you'll be working on. This shows your genuine interest in the role and helps you assess if it's the right fit for you.

✨Be Yourself

Remember, they’re looking for someone who fits into their inclusive culture. Be authentic and let your personality shine through during the interview. This will help you connect better with the hiring manager and the team.

Amgen FSP Clinical Research Associate in Reading
ICON
Location: Reading
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  • Amgen FSP Clinical Research Associate in Reading

    Reading
    Full-Time
    36000 - 60000 ÂŁ / year (est.)
  • I

    ICON

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