Clinical Research Associate - 12 months' monitoring experience required

Clinical Research Associate - 12 months' monitoring experience required

Full-Time 35000 - 45000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Monitor clinical trials, ensuring data integrity and patient safety while collaborating with site staff.
  • Company: Join ICON, a global leader in healthcare intelligence and clinical research.
  • Benefits: Enjoy competitive salary, health coverage, and career development opportunities.
  • Other info: Work in a dynamic environment with a commitment to inclusion and support.
  • Why this job: Make a real impact in advancing innovative treatments and therapies.
  • Qualifications: Must have 12 months' monitoring experience and a degree in a scientific field.

The predicted salary is between 35000 - 45000 £ per year.

CRAICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.

Location - Must be based in the UK. Fully sponsor dedicated.

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.
  • 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:

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%).

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits:

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:

  • Competitive base salary and performance related incentives.
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programmes and wellbeing resources.
  • Learning and development opportunities through structured training and career pathways.

Benefits may vary depending on role and location.

Inclusion and Accessibility: ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Clinical Research Associate - 12 months' monitoring experience required employer: IRE

At ICON, we pride ourselves on being a values-driven organisation that prioritises integrity, collaboration, and inclusion. As a Clinical Research Associate, you will not only contribute to groundbreaking clinical trials but also benefit from a competitive salary, comprehensive health programmes, and robust career development opportunities in a supportive and inclusive work environment. Join us in our mission to bring innovative treatments to patients faster while enjoying the unique advantages of working within a dynamic and growing team in the UK.

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Contact Details:

IRE Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Clinical Research Associate - 12 months' monitoring experience required

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 organisations. A friendly chat can lead to insider info about job openings and even referrals.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of clinical trial processes and ICH-GCP guidelines. We recommend practising common interview questions with a friend to boost your confidence and ensure you shine during the real deal.

Tip Number 3

Showcase your monitoring experience! When you get the chance to speak with recruiters or during interviews, highlight specific examples from your past roles that demonstrate your skills and achievements in clinical trials.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in joining our team at ICON.

We think you need these skills to ace Clinical Research Associate - 12 months' monitoring experience required

Clinical Trial Monitoring
Oncology Trials Experience
Protocol Compliance
Data Integrity
Patient Safety
Site Qualification
Site Initiation

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight your 12 months of monitoring experience and any relevant oncology trials you've worked on. We want to see how your skills align with what we're looking for!

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 you embody our values of integrity, collaboration, agility, and inclusion. Let us know why you want to join our mission at CRAICON.

Showcase Your Skills:In your application, be sure to showcase your strong organisational and communication skills. Mention specific examples where you've ensured protocol compliance and maintained data integrity. We love seeing real-life applications of your expertise!

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, you can explore more about our company culture and benefits while you're there!

How to prepare for a job interview at IRE

Know Your Stuff

Make sure you brush up on your clinical trial processes, regulations, and ICH-GCP guidelines. Being able to discuss these topics confidently will show that you’re not just familiar with the basics but have a solid understanding of what’s required in the role.

Showcase Your Experience

Since they require at least 12 months of monitoring experience, be ready to share specific examples from your past roles. Highlight your contributions to site qualification, monitoring visits, and how you ensured protocol compliance and data integrity.

Emphasise Collaboration

This role involves working closely with investigators and site staff, so be prepared to discuss how you’ve successfully collaborated in previous positions. Share instances where your teamwork led to smoother study conduct or resolved issues effectively.

Ask Insightful Questions

Prepare some thoughtful questions about the company’s approach to clinical trials, especially in oncology. This shows your genuine interest in the role and helps you assess if the company’s values align with yours.