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- Tasks: Lead GCP audits and ensure clinical trials meet top quality standards.
- Company: A leading UK pharmaceutical company focused on quality and compliance.
- Benefits: Competitive salary, career advancement, and the chance to influence quality strategy.
- Why this job: Make a real impact in clinical trials and drive continuous improvement.
- Qualifications: Over 5 years in Clinical Quality Assurance and strong ICH-GCP knowledge.
- Other info: Join a dynamic team dedicated to excellence in healthcare.
The predicted salary is between 48000 - 72000 £ per year.
A leading pharmaceutical company based in the UK is seeking an experienced Clinical Quality Assurance Manager (GCP). This pivotal role involves ensuring clinical trials meet the highest quality standards and regulations. The ideal candidate will have over 5 years' experience in Clinical Quality Assurance, strong knowledge of ICH-GCP, and proven ability to manage quality systems and compliance.
Key responsibilities include:
- Leading GCP audits
- Driving inspection readiness
- Supporting regulatory inspections
An opportunity to influence quality strategy and drive continuous improvement awaits.
GCP Quality Assurance Lead – Clinical Trials in London employer: Planet Pharma
Contact Detail:
Planet Pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land GCP Quality Assurance Lead – Clinical Trials in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who have experience in GCP. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your ICH-GCP knowledge. We recommend creating a list of common interview questions related to quality assurance and practising your answers. Confidence is key!
✨Tip Number 3
Showcase your experience with real-life examples during interviews. We all love a good story, so share how you’ve led GCP audits or improved quality systems in past roles. It’ll make you stand out!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals who want to make a difference in clinical trials.
We think you need these skills to ace GCP Quality Assurance Lead – Clinical Trials in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Clinical Quality Assurance and your knowledge of ICH-GCP. We want to see how your skills align with the role, so don’t be shy about showcasing your relevant achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality assurance in clinical trials and how you can contribute to our team. Keep it engaging and personal – we love to see your personality!
Showcase Your Leadership Skills: Since this role involves leading GCP audits and driving inspection readiness, make sure to highlight any leadership experiences you have. We’re looking for someone who can inspire and guide others, so share those stories!
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 follow the prompts!
How to prepare for a job interview at Planet Pharma
✨Know Your GCP Inside Out
Make sure you brush up on your knowledge of ICH-GCP guidelines. Be prepared to discuss how you've applied these standards in your previous roles, especially in managing quality systems and compliance.
✨Showcase Your Audit Experience
Prepare specific examples of GCP audits you've led or participated in. Highlight any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and attention to detail.
✨Understand the Regulatory Landscape
Familiarise yourself with the latest regulations and trends in clinical trials. Being able to discuss recent changes or upcoming regulations shows that you're proactive and committed to maintaining high-quality standards.
✨Emphasise Continuous Improvement
Think about instances where you've driven quality improvements in your past roles. Be ready to share how you identified areas for enhancement and the impact your initiatives had on trial outcomes.
