At a Glance
- Tasks: Support early-phase clinical trials by monitoring participants and conducting study-specific procedures.
- Company: Join a global CRO with a focus on innovative clinical research.
- Benefits: Competitive hourly rate, contract position with potential extension, and valuable experience in clinical trials.
- Why this job: Make a real difference in patient care while gaining hands-on experience in clinical research.
- Qualifications: NMC registered with prior exposure to clinical trials and strong understanding of clinical protocols.
- Other info: Night shifts (3 per week) in a dynamic research environment with growth opportunities.
The predicted salary is between 15 - 22 Β£ per hour.
CPL Life Sciences are currently partnering a global CRO who are actively recruiting two Clinical Research Nurses to support a high-volume early-phase clinical trials unit located at a North-West London hospital site. This is a contract position from March to July, with potential extension due to peak workload demands. The role involves working night shifts (3 per week) and supporting multiple early-phase studies across a range of therapy areas.
Key responsibilities include:
- Monitoring trial participants overnight
- Conducting study-specific procedures in accordance with clinical protocols
- Administering investigational medicinal products where required
- Recording observations, and responding to any adverse events
- Ensuring accurate documentation and compliance with GCP, regulatory, and safety standards
- Delivering high-quality patient care in a research environment
Candidates must be NMC registered and have prior exposure to clinical trials or research settings with a strong understanding of clinical protocols. This role is equivalent to NHS Band 5β6, with a competitive hourly rate available. Applicants working full-time for other CROs cannot be considered due to conflict of interest.
If this is of interest to you then please apply here, or email your CV to sarah.phillips@cpl.com for further information.
Clinical Research Nurse employer: CPL
Contact Detail:
CPL Recruiting Team
StudySmarter Expert Advice π€«
We think this is how you could land Clinical Research Nurse
β¨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who might know about opportunities at CROs. A friendly chat can sometimes lead to job openings that aren't even advertised yet.
β¨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical protocols and GCP guidelines. We want you to feel confident discussing your experience with trial participants and how you handle adverse events. Practice makes perfect!
β¨Tip Number 3
Showcase your passion for patient care and research during interviews. Share specific examples of how you've contributed to high-quality patient care in previous roles. This will help you stand out as a candidate who truly cares about the work.
β¨Tip Number 4
Don't forget to apply through our website! Itβs the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive and eager to join our team.
We think you need these skills to ace Clinical Research Nurse
Some tips for your application π«‘
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Nurse role. Highlight your NMC registration and any relevant experience in clinical trials or research settings. We want to see how your background aligns with the responsibilities outlined in the job description!
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 make you a great fit for the role. We love seeing genuine enthusiasm, so let your personality come through!
Showcase Relevant Skills: In your application, be sure to showcase skills that are crucial for the role, like monitoring trial participants and conducting study-specific procedures. Weβre looking for candidates who can demonstrate their understanding of clinical protocols and GCP compliance.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications better and ensures you donβt miss out on any important updates. Plus, itβs super easy!
How to prepare for a job interview at CPL
β¨Know Your Clinical Protocols
Make sure you brush up on the clinical protocols relevant to the role. Understanding the specifics of early-phase trials and the procedures you'll be conducting will show your potential employer that you're not just familiar with the basics, but that youβre ready to hit the ground running.
β¨Highlight Your NMC Registration
Since being NMC registered is a must for this position, donβt forget to emphasise your registration during the interview. Be prepared to discuss how your qualifications and experience align with the responsibilities of monitoring trial participants and ensuring compliance with GCP standards.
β¨Showcase Your Experience
If you've worked in clinical trials or research settings before, make sure to share specific examples of your past experiences. Talk about the types of studies you've been involved in, any challenges you faced, and how you overcame them. This will demonstrate your capability and adaptability in a fast-paced environment.
β¨Prepare for Night Shift Questions
Since this role involves working night shifts, be ready to discuss your availability and how you manage working at unconventional hours. Share any previous experience with night shifts and how you maintain your performance and well-being during those hours.