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- Tasks: Coordinate audits and ensure clinical quality systems are inspection-ready.
- Company: Global biopharmaceutical organisation with a focus on innovation.
- Benefits: Hybrid work environment, competitive salary, and opportunities for professional growth.
- Why this job: Join a dynamic team and make a real impact in clinical quality.
- Qualifications: 3-5 years of clinical quality experience in pharma or CRO.
- Other info: Exciting role with a chance to stay updated on regulatory changes.
The predicted salary is between 36000 - 60000 £ per year.
A global biopharmaceutical organization in the UK is seeking a Clinical Quality Coordinator to act as the Audit Host and Regulatory Intelligence Coordinator. The successful candidate will ensure clinical quality systems are inspection-ready and comply with GCP regulations.
Responsibilities include:
- Coordinating audits
- Managing CAPAs
- Monitoring regulatory updates
Ideal candidates will have 3–5 years of clinical quality experience in a pharma or CRO environment. This role offers a hybrid work environment.
Clinical Quality Audit Host & Regulatory Intelligence Lead in Slough employer: Planet Pharma
Contact Detail:
Planet Pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Quality Audit Host & Regulatory Intelligence Lead in Slough
✨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 Quality Coordinator role.
✨Tip Number 2
Prepare for interviews by brushing up on GCP regulations and recent regulatory updates. We recommend creating a cheat sheet of key points to discuss, so you can impress your interviewers with your knowledge and confidence.
✨Tip Number 3
Showcase your experience with CAPAs and audits during interviews. We suggest using the STAR method (Situation, Task, Action, Result) to structure your answers, making it easier for interviewers to see your impact in previous roles.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of resources to help you prepare and stand out. Plus, applying directly shows your enthusiasm for the role and the company.
We think you need these skills to ace Clinical Quality Audit Host & Regulatory Intelligence Lead in Slough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your clinical quality experience, especially in pharma or CRO environments. We want to see how your skills align with the role of Audit Host and Regulatory Intelligence Coordinator.
Showcase Relevant Experience: When writing your cover letter, focus on your experience with audits, CAPAs, and GCP regulations. We love seeing specific examples that demonstrate your expertise and how you can contribute to our team.
Be Clear and Concise: Keep your application straightforward and to the point. We appreciate clarity, so avoid jargon and make sure your key achievements stand out. This helps us quickly see why you’re a great fit!
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. We can’t wait to hear from you!
How to prepare for a job interview at Planet Pharma
✨Know Your GCP Regulations
Make sure you brush up on Good Clinical Practice (GCP) regulations before the interview. Being able to discuss how you've ensured compliance in previous roles will show that you're not just familiar with the standards, but that you can apply them effectively.
✨Prepare for Audit Scenarios
Think of specific examples from your past experience where you coordinated audits or managed CAPAs. Be ready to explain your approach and the outcomes. This will demonstrate your hands-on experience and problem-solving skills in a clinical quality context.
✨Stay Updated on Regulatory Changes
Since the role involves monitoring regulatory updates, it’s crucial to show that you’re proactive about staying informed. Mention any recent changes in regulations that you’ve followed and how they might impact clinical quality systems.
✨Emphasise Your Teamwork Skills
In a hybrid work environment, collaboration is key. Be prepared to discuss how you've worked effectively with cross-functional teams in the past. Highlight your communication skills and how you ensure everyone is aligned during audits and regulatory processes.
