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- Tasks: Monitor clinical studies and ensure compliance with Good Clinical Practices.
- Company: Global CRO supporting top Pharmaceutical & Biotech companies.
- Benefits: Competitive salary, career growth, and a dynamic work environment.
- Why this job: Join a team making a real difference in clinical research.
- Qualifications: Bachelor's in life-science and at least 1 year of CRA experience.
- Other info: Exciting opportunities for professional development in a supportive culture.
The predicted salary is between 36000 - 60000 £ per year.
Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate in London.
Job Overview:
- Monitoring clinical studies in phases II-III
- Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
- Identification, qualification and initiation of investigators and their sites.
- Supervising study conduct according to GCP requirements and all applicable laws.
Key Requirements:
- Bachelor degree in life-science
- Min 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in UK
- Experience in commercial studies
- Experience with site initiation, site close out
- Experience in clinical studies phase II-III
- Fluent English
- Excellent communication skills
- A full clean drivers license
FTE: 1.0
If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on 0044 (0) 207 421 0000 or email info@life-science.co.uk
Lead Clinical Research Associate – London, UK in City of London employer: Resourcing Life Science
Contact Detail:
Resourcing Life Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Lead Clinical Research Associate – London, UK in City of London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Show them you’re genuinely interested in their work and how you can contribute. We recommend practising common interview questions with a friend or even in front of the mirror!
✨Tip Number 3
Follow up after interviews! A simple thank-you email can go a long way in keeping you top of mind. We suggest mentioning something specific from your conversation to make it personal.
✨Tip Number 4
Don’t forget to apply through our website! It’s super easy and ensures your application gets the attention it deserves. Plus, we’re always here to help if you have any questions along the way!
We think you need these skills to ace Lead Clinical Research Associate – London, UK in City of London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Lead Clinical Research Associate role. Highlight your monitoring experience and any relevant skills that match the job description. 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 experience aligns with our needs. Keep it concise but engaging – we love a good story!
Showcase Your Communication Skills: Since excellent communication is key in this role, make sure your application reflects that. Use clear and professional language, and don’t forget to proofread for any typos or errors. We appreciate attention to detail!
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’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Resourcing Life Science
✨Know Your Clinical Research Basics
Make sure you brush up on your knowledge of Good Clinical Practices (GCP) and the phases of clinical studies, especially phases II-III. Being able to discuss these topics confidently will show that you’re not just familiar with the role but also passionate about it.
✨Showcase Your Monitoring Experience
Prepare specific examples from your previous monitoring experience as a CRA. Highlight any challenges you faced and how you overcame them, particularly in site initiation and close-out processes. This will demonstrate your problem-solving skills and adaptability.
✨Communicate Clearly and Effectively
Since excellent communication skills are a key requirement, practice articulating your thoughts clearly. You might want to do mock interviews with friends or family to refine your responses and ensure you can convey your ideas succinctly.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions! Inquire about the company’s approach to clinical trials or their expectations for the role. This shows your genuine interest and helps you assess if the company is the right fit for you.