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- Tasks: Support clinical studies from planning to closeout while ensuring compliance and managing documents.
- Company: Leading biopharmaceutical company in the UK with a focus on innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Join a dynamic team and contribute to groundbreaking clinical research that makes a difference.
- Qualifications: BS/BA in a scientific field and two years of clinical trials experience required.
- Other info: Ideal for those passionate about science and making an impact in healthcare.
The predicted salary is between 36000 - 60000 £ per year.
A leading biopharmaceutical company in the United Kingdom is seeking a Clinical Study Coordinator to support the operational activities for planning, initiation, conduct, and closeout of assigned clinical studies. The ideal candidate will have a BS/BA in a scientific field and at least two years of experience in clinical trials.
Responsibilities include:
- Managing document collections
- Ensuring compliance with guidelines
- Collaborating with Clinical Trial Managers
Strong analytical and communication skills are essential for success in this role.
Clinical Trials Operations & Compliance Specialist in City of Westminster employer: Neurocrine Biosciences
Contact Detail:
Neurocrine Biosciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trials Operations & Compliance Specialist in City of Westminster
✨Tip Number 1
Network like a pro! Reach out to professionals in the biopharmaceutical field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Clinical Trials Operations & Compliance Specialist role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical trial regulations and compliance. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence!
✨Tip Number 3
Showcase your analytical skills during interviews. Be ready to discuss specific examples from your past experiences where you successfully managed document collections or ensured compliance. We want to see how you can bring that expertise to our team!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Clinical Trials Operations & Compliance Specialist in City of Westminster
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in clinical trials and any relevant scientific qualifications. We want to see how your background aligns with the role of Clinical Study Coordinator, so don’t hold back on showcasing your skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical trials and how your previous experiences make you a great fit for our team. Let us know what excites you about this opportunity!
Showcase Your Compliance Knowledge: Since compliance is key in this role, be sure to mention any specific guidelines or regulations you’re familiar with. We love candidates who can demonstrate their understanding of the compliance landscape in clinical studies.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Neurocrine Biosciences
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trials and the specific regulations that govern them. Familiarise yourself with the latest guidelines and compliance standards, as this will show your potential employer that you're serious about the role.
✨Showcase Your Experience
Prepare to discuss your previous experience in clinical trials in detail. Think of specific examples where you've managed document collections or collaborated with Clinical Trial Managers. This will help demonstrate your hands-on experience and how it aligns with the job requirements.
✨Communicate Clearly
Strong communication skills are a must for this role. Practice articulating your thoughts clearly and concisely. You might even want to do a mock interview with a friend to get comfortable discussing complex topics in an easy-to-understand way.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions! Inquire about the company’s approach to clinical trial compliance or how they support their Clinical Study Coordinators. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
