At a Glance
- 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 England 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 England
✨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 practicing your answers. Confidence is key!
✨Tip Number 3
Showcase your experience with real-life examples. When discussing your past roles, highlight specific instances where you led GCP audits or improved quality systems. This will demonstrate your hands-on expertise.
✨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 GCP Quality Assurance Lead – Clinical Trials in England
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
Be ready to share specific examples of GCP audits you've led. Highlight any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and leadership in quality assurance.
✨Prepare for Regulatory Inspections
Think about your experience with regulatory inspections and how you ensured inspection readiness. Discuss strategies you've implemented to maintain compliance and how you’ve supported teams during inspections.
✨Emphasise Continuous Improvement
Talk about initiatives you've led or contributed to that drove continuous improvement in clinical trials. This shows your proactive approach and ability to influence quality strategy, which is key for the role.