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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.
- Other info: Exciting opportunity for those passionate about clinical research.
- 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.
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.
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
Lead Clinical Research Associate 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 UK in City of 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 forget to showcase your communication skills! During interviews, be clear and concise when explaining your past experiences. Remember, they want to see how well you can convey complex information.
✨Tip Number 4
Apply through our website for a smoother process! It’s super easy, and we’re here to help if you hit any snags. Plus, it shows you’re serious about landing that Lead Clinical Research Associate role!
We think you need these skills to ace Lead Clinical Research Associate 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 client's 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 get the best chance at landing an interview with 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 role but also passionate about it.
✨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. This will help demonstrate your hands-on knowledge and how it aligns with what the company is looking for.
✨Communicate Clearly
Since excellent communication skills are a key requirement, practice articulating your thoughts clearly and concisely. You might even want to do a mock interview with a friend to get comfortable discussing your experiences and answering potential questions.
✨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 CRA role. This shows your interest and helps you gauge if the company is the right fit for you.