At a Glance
- Tasks: Coordinate clinical trials and ensure compliance while collecting and analysing critical data.
- Company: Join ICON, a global leader in healthcare intelligence and clinical research.
- Benefits: Enjoy competitive salary, health coverage, and career development opportunities.
- Other info: Be part of a diverse team that values integrity, collaboration, and inclusion.
- Why this job: Make a real impact on patient care by bringing new treatments to market faster.
- Qualifications: University degree in life sciences and at least 12 months of monitoring experience.
The predicted salary is between 30000 - 40000 € per year.
ICON 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.
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON (at either CRA I or II level). As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data. This role is dedicated to one of our valued sponsors.
What you will be doing:
- 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.
- Developing and maintaining strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
- Ensuring patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.
Your profile:
- University degree in medicine, science/lifesciences or nursing.
- At least 12 months of independent on-site monitoring experience for a CRO or pharmaceutical company.
- 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.
- Ability to travel as required of the time domestic - fly and drive across the UK and should possess a valid driver's license.
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 II 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 thrive in a dynamic work culture that fosters professional growth through structured training and development opportunities, all while contributing to meaningful healthcare advancements. Our competitive benefits package, including health programmes and performance incentives, ensures that our employees are well-supported in both their personal and professional lives.
StudySmarter Expert Advice🤫
We think this is how you could land Cra II
✨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 convey complex information clearly. Try mock interviews with friends or use online resources to refine your verbal and written communication.
✨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 Cra II
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the CRA role. Highlight your relevant experience, especially any independent on-site monitoring you've done. 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, and inclusion. Let us know why you want to join our team at ICON.
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!
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to find all the details you need about the role and our company culture!
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 Experience
Prepare specific examples from your previous monitoring experience that highlight your ability to manage studies independently. Think about challenges you've faced and how you overcame them, as this will demonstrate your problem-solving skills and resilience.
✨Build Rapport
Since collaboration is key in this role, practice how you'll build relationships with stakeholders and site staff. Be ready to discuss how you’ve successfully worked with others in the past and how you plan to foster those connections at ICON.
✨Ask Insightful Questions
Prepare thoughtful questions about the company culture, team dynamics, and specific projects you might be involved in. This shows your genuine interest in the role and helps you assess if ICON is the right fit for you.
