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- Tasks: Monitor clinical trials in real-time and ensure data integrity.
- Company: Fortrea, a leader in clinical research based in Leeds.
- Benefits: Flexible working arrangements and a permanent full-time role.
- Other info: Relocation within Yorkshire is ideal for this collaborative position.
- Why this job: Join a dynamic team and contribute to groundbreaking clinical studies.
- Qualifications: Experience in clinical research or site-based roles is preferred.
The predicted salary is between 30000 - 40000 £ per year.
Fortrea in Leeds is hiring Clinical Research Associates (CRA I and CRA II) for Phase I–Ib studies. Ideal candidates will have relevant experience in clinical research or site-based roles, with the position offering a blend of modern clinical technology and on-site collaboration. This full-time, permanent role emphasizes data integrity and protocol compliance. Relocation within Yorkshire is ideal, with flexible working arrangements available.
Onsite Early-Phase CRA II: Real-Time Trial Monitoring employer: Fortrea
Contact Detail:
Fortrea Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Onsite Early-Phase CRA II: Real-Time Trial Monitoring
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at Fortrea or similar companies. A friendly chat can sometimes lead to insider info about job openings or even a referral!
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of Phase I–Ib studies and the latest in clinical technology. We want you to shine when discussing data integrity and protocol compliance, so make sure you’ve got some solid examples ready to share.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It shows your enthusiasm for the role and keeps you fresh in their minds.
✨Tip Number 4
Apply through our website for the best chance of landing that CRA II role! We’re all about making the application process smooth and straightforward, so don’t miss out on the opportunity to showcase your skills directly to us.
We think you need these skills to ace Onsite Early-Phase CRA II: Real-Time Trial Monitoring
Some tips for your application 🫡
Show Your Experience: When you're writing your application, make sure to highlight any relevant experience you have in clinical research or site-based roles. We want to see how your background aligns with the responsibilities of the CRA II position.
Be Clear and Concise: Keep your application straightforward and to the point. We appreciate clarity, so avoid jargon and long-winded explanations. Just tell us what we need to know about your skills and experiences!
Tailor Your Application: Make sure to customise your application for the role at Fortrea. Mention specific aspects of the job description that excite you and how you can contribute to the team. We love seeing genuine interest!
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Fortrea
✨Know Your Clinical Research Stuff
Make sure you brush up on your knowledge of clinical research, especially Phase I–Ib studies. Be ready to discuss your previous experiences and how they relate to the role at Fortrea. This shows that you’re not just familiar with the basics but also understand the nuances of the field.
✨Show Off Your Tech Savvy
Since the role involves modern clinical technology, be prepared to talk about any relevant tools or software you've used in past roles. Highlighting your ability to adapt to new technologies will demonstrate that you can thrive in a tech-driven environment.
✨Emphasise Data Integrity
Data integrity is crucial in clinical trials. Be ready to discuss how you ensure compliance with protocols and maintain data accuracy in your work. Sharing specific examples will help illustrate your commitment to high standards in clinical research.
✨Be Ready for On-Site Collaboration
As this role involves on-site collaboration, think about your teamwork experiences. Prepare to share how you’ve successfully worked with others in a clinical setting, as well as how you handle challenges that arise in team dynamics.