CRA

Full-Time 35000 - 45000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Monitor clinical trials and ensure high-quality outcomes while collaborating with your team.
  • 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 from home with flexible travel to hospital sites across the UK.
  • Why this job: Make a real difference in patient care by bringing new treatments to market faster.
  • Qualifications: Degree in medicine or science and UK clinical trial monitoring experience required.

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

UKICON 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.

As a UK home-based CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality monitoring 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 UK-based 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 to hospital sites in the UK as required (approximately 40%), and holding a driving licence.

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. Visit our careers site to read more about the benefits ICON offers.

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.

CRA employer: IRE

At ICON, we pride ourselves on being a values-driven organisation that prioritises integrity, collaboration, and inclusion. As a home-based Clinical Research Associate in the UK, you will enjoy a supportive work culture that fosters professional growth through structured training and development opportunities, alongside a competitive benefits package that includes health and wellbeing programmes. Join us in our mission to bring new medicines to patients faster while working in a flexible environment that values your contributions and promotes a healthy work-life balance.

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Contact Details:

IRE Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land CRA

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. The more people you know, the better your chances of landing that CRA role!

Tip Number 2

Prepare for interviews by researching ICON and understanding their values. Be ready to discuss how your experience aligns with their mission to bring new medicines to patients faster. Show them you're not just a fit on paper but also in spirit!

Tip Number 3

Practice your communication skills! As a CRA, you'll need to build strong relationships with stakeholders. Role-play common interview scenarios with a friend to boost your confidence and refine your responses.

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 the ICON team. Let's get you that CRA position!

We think you need these skills to ace CRA

Clinical Trial Monitoring
Knowledge of ICH-GCP Guidelines
Medical Data Evaluation
Study Documentation Management
Stakeholder Relationship Management
Excellent Written Communication
Excellent Verbal Communication

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the CRA role at ICON. 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!

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 values align with ours. Remember, we love integrity, collaboration, and inclusion!

Showcase Your Communication Skills:Since excellent written communication is key for this role, make sure your application is clear and concise. We appreciate good social skills, so let your personality come through while keeping it professional.

Apply Through Our Website:Don’t forget to apply through our careers site! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, you can check out all the benefits we offer!

How to prepare for a job interview at IRE

Know Your Stuff

Make sure you brush up on your knowledge of ICH-GCP guidelines and clinical trial processes. Being able to discuss these topics confidently will show that you're not just familiar with the basics, but that you truly understand the intricacies of the role.

Showcase Your Communication Skills

Since this role involves building strong relationships with stakeholders and site staff, practice articulating your thoughts clearly. Prepare examples of how you've effectively communicated in past roles, especially when dealing with queries or challenges.

Demonstrate Your Agility

Be ready to discuss how you've adapted to changes in previous projects. Highlight instances where you've had to think on your feet or adjust your approach to meet deadlines or overcome obstacles—this aligns perfectly with the agility value at ICON.

Ask Insightful Questions

Prepare thoughtful questions about the company's culture, team dynamics, and specific projects. This not only shows your interest in the role but also helps you gauge if the company is the right fit for you. Plus, it demonstrates your proactive nature!