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- Tasks: Oversee GCP activities and lead audits for clinical trials in a dynamic pharmaceutical environment.
- Company: Major global research-driven pharmaceutical company focused on neurology and oncology.
- Benefits: Competitive salary, career growth opportunities, and impactful work in healthcare.
- Why this job: Make a real difference in patient safety and data integrity while leading quality assurance efforts.
- Qualifications: Experience in quality assurance and strong leadership skills in clinical settings.
- Other info: High visibility role with significant impact potential in a collaborative team.
The predicted salary is between 36000 - 60000 £ 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.
Main duties/responsibilities:
- 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 England 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 England
✨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 a lead on that Associate Director role!
✨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 or networking chat, drop a quick thank-you email. It keeps you fresh in their minds and shows your enthusiasm for the role. Plus, it’s a great way to reiterate your interest in the position.
✨Tip Number 4
Apply through our website! We make it easy for you to showcase your skills and experience directly to the hiring team. Plus, it gives you a better chance of standing out in the application process. So, don’t wait – get your CV in there!
We think you need these skills to ace Associate Director Quality Assurance in England
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 outlined 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 contributed to successful clinical trials. 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 shows you’re serious about joining our team!
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. Since the role involves overseeing GCP activities, being well-versed in these regulations will show your expertise and commitment to quality assurance.
✨Prepare for Scenario-Based Questions
Expect questions that ask how you would handle specific situations, like managing audits or dealing with non-compliance. Think of examples from your past experiences where you successfully navigated similar challenges.
✨Showcase Your Cross-Functional Collaboration Skills
This position requires managing relationships across various teams. Be ready to discuss how you've effectively collaborated with different departments in previous roles, highlighting your communication and leadership skills.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions prepared. Inquire about the company's approach to quality improvement or how they support the training and development of their QA team. This shows your genuine interest in the role and the company.
