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- Tasks: Oversee GCP activities, lead audits, and ensure high-quality clinical trial execution.
- Company: Global research-driven pharmaceutical company focused on neurology and oncology.
- Benefits: Permanent position with high visibility and significant impact potential.
- Why this job: Join a team that prioritises patient safety and data integrity in clinical trials.
- Qualifications: Experience in quality assurance and strong leadership skills required.
- Other info: Opportunity for professional growth and collaboration with cross-functional teams.
The predicted salary is between 43200 - 72000 £ per year.
I'm working with a major global research‐driven pharmaceutical company best known for its work in neurology and oncology. They are looking for an Associate Director, Quality Assurance to join their team on a permanent basis.
The successful candidate will oversee GCP activities, CROs and Investigator Sites, lead GCP audits and inspection management activities; will ensure high quality execution of clinical trials from first in human through commercial marketing authorizations; will manage cross functional relationships and be the Lead Quality Assurance representative with both internal and external stakeholders. This is a high visibility position with great impact potential.
- Representing CQA at internal, cross functional team meetings
- Supporting the training and development of CQA colleagues
- Proactively provide GCP QA support for clinical development activities to protect patient safety & well being, maintain data integrity, and support operational excellence
- Independently conduct Clinical Investigator Site Audits, GCP Document Audits (Clinical Study Reports and Trial Master Files), internal Process Audits and Vendor/System audits
- Acting as CQA Lead for clinical studies, drafting and managing Audit Plans and Audit reports
- Facilitate ongoing quality improvement through communication of audit results, CAPAs and GCP guidance and consultation to clinical teams
If this is something you would be interested in exploring send your CV to jamie.keith@cpl.com
Associate Director Quality Assurance in London employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director Quality Assurance in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical industry, especially those involved in quality assurance. Use platforms like LinkedIn to connect and engage with them; you never know who might have the inside scoop on job openings.
✨Tip Number 2
Prepare for interviews by brushing up on your GCP knowledge and audit experience. Be ready to discuss specific examples of how you've ensured data integrity and patient safety in past roles. This will show you're not just a fit on paper but also in practice!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds and shows your enthusiasm for the position.
✨Tip Number 4
Apply through our website! We often have exclusive listings that might not be found elsewhere. Plus, it’s a great way to ensure your application gets the attention it deserves from our hiring team.
We think you need these skills to ace Associate Director Quality Assurance in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Associate Director, Quality Assurance role. Highlight your experience with GCP activities and any relevant audits you've conducted. We want to see how your background aligns with the responsibilities mentioned in the job description.
Showcase Your Impact: In your application, don’t just list your duties; showcase your impact! Use specific examples of how you’ve improved quality assurance processes or enhanced patient safety in previous roles. This will help us see the value you can bring to our team.
Be Clear and Concise: When writing your application, keep it clear and concise. Avoid jargon unless it's relevant to the role. We appreciate straightforward communication, so make sure your key points stand out without unnecessary fluff.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications better and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your GCP Inside Out
Make sure you brush up on Good Clinical Practice (GCP) guidelines before the interview. Be ready to discuss how you've applied these principles in your previous roles, especially in relation to clinical trials and audits.
✨Showcase Your Leadership Skills
As an Associate Director, you'll need to demonstrate strong leadership capabilities. Prepare examples of how you've led teams or projects, particularly in quality assurance settings, and how you've managed cross-functional relationships effectively.
✨Prepare for Scenario-Based Questions
Expect questions that ask you to solve hypothetical problems related to GCP audits or inspection management. Think through potential scenarios and how you would handle them, focusing on maintaining patient safety and data integrity.
✨Highlight Your Communication Skills
Since this role involves liaising with various stakeholders, be prepared to discuss how you communicate complex quality assurance concepts clearly. Share examples of how you've facilitated training or communicated audit results to ensure understanding and compliance.
