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For Companies At a Glance
- 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: Make a real impact in clinical research and contribute to groundbreaking studies.
- Qualifications: Bachelor's in life-science and at least 1 year of CRA experience.
- Other info: Exciting opportunity for those passionate about clinical research.
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 UK in 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 UK in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at CROs or in pharma. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of Good Clinical Practices and the latest trends in clinical research. We want you to shine when discussing your experience with phases II-III studies!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your career goals. Check out our website for tailored opportunities that match your skills as a Lead Clinical Research Associate.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind for hiring managers. Plus, it shows your enthusiasm for the role and the company.
We think you need these skills to ace Lead Clinical Research Associate UK in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical research, especially your monitoring experience. We want to see how your background aligns with the role of a Lead Clinical Research Associate.
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 the perfect fit for our team. We love seeing genuine enthusiasm!
Showcase Your Communication Skills: Since excellent communication is key in this role, make sure your application reflects that. Whether it's through clear language in your CV or a well-structured cover letter, we want to see your ability to convey information effectively.
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 don’t miss out on any important updates from us!
How to prepare for a job interview at Resourcing Life Science
✨Know Your Stuff
Make sure you brush up on your knowledge of Good Clinical Practices (GCP) and the specific phases of clinical studies, especially II-III. Being able to discuss these topics confidently will show that you're not just familiar with the basics but also understand the nuances of the role.
✨Showcase Your Experience
Prepare to talk about your previous monitoring experience in detail. Highlight specific projects you've worked on, particularly any site initiation or close-out experiences. Use examples that demonstrate your ability to ensure compliance and maintain investigator integrity.
✨Communicate Clearly
Since excellent communication skills are a key requirement, practice articulating your thoughts clearly and concisely. Consider doing mock interviews with a friend or colleague to refine your responses and ensure you can convey your ideas effectively.
✨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 how they support their CRAs in professional development. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
