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- Tasks: Enhance quality frameworks and ensure compliance across clinical projects.
- Company: Leading contract research organisation in the UK with a supportive team culture.
- Benefits: Opportunity to make a significant impact and develop your career.
- Why this job: Join a dynamic team and shape the future of clinical research.
- Qualifications: Over a decade of clinical research experience and strong regulatory knowledge.
- Other info: Ideal for those passionate about quality assurance in healthcare.
The predicted salary is between 48000 - 72000 £ per year.
A leading contract research organization in the UK is seeking a QA & Compliance Manager to enhance their quality framework across clinical projects. This role demands extensive experience in quality assurance within clinical trials, with responsibilities including:
- The development of a Quality Management System
- Compliance assurance
- Managing audits
The ideal candidate will possess over a decade of clinical research experience and a solid regulatory background. This position offers a chance to make a significant impact in a supportive team environment.
Senior QA & Compliance Lead — Global CRO, Autonomy in London employer: CYTE Global
Contact Detail:
CYTE Global Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QA & Compliance Lead — Global CRO, Autonomy in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the hunt for a Senior QA & Compliance Lead role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of quality management systems and compliance regulations. We recommend creating a list of common interview questions related to QA in clinical trials and practising your responses. Confidence is key!
✨Tip Number 3
Showcase your experience! When you get the chance to chat with potential employers, highlight your decade of clinical research experience and any successful audits you've managed. We want to see you shine and demonstrate how you can enhance their quality framework.
✨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 love seeing familiar faces from our community making strides in their careers!
We think you need these skills to ace Senior QA & Compliance Lead — Global CRO, Autonomy in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your extensive experience in quality assurance and clinical trials. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects and achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about enhancing quality frameworks and how your decade of experience can contribute to our team. Keep it engaging and personal!
Showcase Your Regulatory Knowledge: Since this role requires a solid regulatory background, make sure to mention any specific regulations or guidelines you’ve worked with. We love seeing candidates who are well-versed in compliance and can navigate the complexities of clinical research.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves!
How to prepare for a job interview at CYTE Global
✨Know Your Quality Frameworks
Make sure you brush up on the various quality frameworks relevant to clinical trials. Be prepared to discuss how you've developed or enhanced these systems in your previous roles. This shows that you understand the importance of compliance and can bring valuable insights to the team.
✨Showcase Your Audit Experience
Since managing audits is a key responsibility, come ready with examples of audits you've conducted or participated in. Highlight any challenges you faced and how you overcame them. This will demonstrate your hands-on experience and problem-solving skills.
✨Regulatory Knowledge is Key
Familiarise yourself with the latest regulations and guidelines in clinical research. Be prepared to discuss how you've ensured compliance in past projects. This will show that you’re not just experienced but also up-to-date with industry standards.
✨Emphasise Team Collaboration
This role is in a supportive team environment, so be ready to talk about how you've worked effectively within teams. Share specific examples of how you’ve collaborated with others to enhance quality assurance processes. This will highlight your ability to fit into their culture.
