At a Glance
- Tasks: Join a dynamic team to lead clinical trials for innovative diagnostics.
- Company: ICON, a global leader in healthcare intelligence and clinical research.
- Benefits: Competitive salary, health coverage, career development, and wellbeing programmes.
- Other info: Inclusive workplace with opportunities for growth and travel.
- Why this job: Make a real impact in healthcare by bringing new treatments to patients faster.
- Qualifications: Degree in medicine or science, with lab experience in in vitro diagnostics.
The predicted salary is between 30000 - 40000 £ per year.
IVD 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. As a UK home-based In Vitro Diagnostics CRA at ICON, you will contribute to our clinical trial operations function, working in an enthusiastic, dynamic team. This is a unique opportunity to move from a lab-based setting into a CRA role, embedded into a blue chip clinical diagnostics project, you will join your colleagues in leading the design, planning, co-ordinating and conducting of all activities involved in initiating, monitoring and completing clinical research studies for in vitro diagnostics.
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:
- ensuring studies are conducted according to study protocols, operating procedures, and good clinical practice.
- validating product performance claims
- supplying data for critical Regulatory submissions
- defining the functional and clinical utility of investigation products
- understanding and implementing federal regulations, helping to roll out SOPs in order to ensure that studies are adhering to FDA regulations, GCP, IVD directives and client policy.
Your Profile:
You will bring relevant In Vitro Diagnostics experience, ideally from a laboratory background, along with the following qualifications and skills.
Required qualifications and experience:
- University degree in medicine, science, or equivalent
- Practical knowledge of in vitro diagnostics and clinical trial processes
- Excellent written and verbal communication in English
- Good social skills enabling you to deal with queries in a timely manner
- Willingness to travel as required from your UK base (occasionally internationally)
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.
Clinical Research Associate 1 employer: IRE
ICON is an exceptional employer that prioritises integrity, collaboration, and inclusion, making it a fantastic place for Clinical Research Associates to thrive. With a competitive salary, comprehensive health benefits, and robust career development opportunities, employees are supported in their professional growth while contributing to meaningful clinical research projects. The home-based role offers flexibility and the chance to work within a dynamic team dedicated to advancing healthcare solutions.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate 1
✨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 practising common CRA questions. We recommend doing mock interviews with friends or using online resources. The more comfortable you are, the better you'll perform when it counts!
✨Tip Number 3
Showcase your passion for clinical research during interviews. Share specific examples from your lab experience that highlight your skills and how they relate to the CRA role. Let your enthusiasm shine through!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, you’ll find all the latest opportunities tailored to your skills and interests right there.
We think you need these skills to ace Clinical Research Associate 1
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight your relevant experience in in vitro diagnostics and any lab work you've done. We want to see how your background fits 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 your skills align with our values of integrity, collaboration, and agility. Let us know why you want to join our dynamic team!
Showcase Your Communication Skills:Since excellent written and verbal communication is key for this role, make sure your application reflects that. Keep your language clear and professional, and don’t forget to proofread for any typos or errors before hitting send!
Apply Through Our Website:We encourage you to apply through our website for the best chance of success. It’s super easy, and you’ll be able to find all the details you need about the role and our company. Plus, we love seeing applications come directly from our site!
How to prepare for a job interview at IRE
✨Know Your Stuff
Make sure you brush up on your knowledge of in vitro diagnostics and clinical trial processes. Familiarise yourself with the latest regulations and guidelines, especially those related to FDA and GCP. This will show that you're not just interested in the role but also committed to delivering high-quality work.
✨Showcase Your Communication Skills
Since excellent written and verbal communication is key for this role, practice articulating your thoughts clearly. Prepare to discuss how you've effectively communicated in past roles, especially when dealing with queries or collaborating with teams. This will help demonstrate your social skills and ability to work well with others.
✨Be Ready to Discuss Your Experience
Think about your previous lab-based experiences and how they relate to the CRA role. Be prepared to share specific examples of how you've contributed to projects, validated product performance claims, or adhered to protocols. This will help the interviewers see how your background aligns with their needs.
✨Emphasise Your Adaptability
Highlight your willingness to travel and adapt to new environments, as this role may require occasional international travel. Share any experiences where you've had to be agile and flexible in your work, which aligns with the values of collaboration and agility that the company holds dear.
