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- Tasks: Lead quality assurance for clinical trials and ensure high standards in patient safety and data integrity.
- 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 values quality and makes a difference in healthcare.
- Qualifications: Experience in GCP activities and strong leadership skills required.
- Other info: Opportunity for professional growth in a dynamic and impactful environment.
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
Associate Director Quality Assurance in Waterford 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 Waterford
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those involved in quality assurance. 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 GCP guidelines and recent trends in clinical trials. We want you to be the go-to expert in the room, so practice articulating how your experience aligns with the role.
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications through our website. A quick email expressing your enthusiasm can keep you top of mind for hiring managers.
✨Tip Number 4
Showcase your leadership skills! In interviews, highlight examples where you've led audits or managed cross-functional teams. We want to see how you can make an impact in this high visibility role.
We think you need these skills to ace Associate Director Quality Assurance in Waterford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Associate Director, Quality Assurance role. Highlight your experience in 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 processes or ensured compliance 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 that gets to the point, so make every word count!
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 keen on 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. Be prepared 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 abilities. Think of examples where you've led teams or projects, particularly in quality assurance settings, and be ready to share these during the interview.
✨Prepare for Scenario-Based Questions
Expect questions that ask how you would handle specific situations, such as managing a GCP audit or dealing with non-compliance issues. Practise articulating your thought process and decision-making strategies.
✨Highlight Cross-Functional Collaboration
This role involves working with various stakeholders. Be ready to discuss your experience in managing cross-functional relationships and how you've successfully communicated quality assurance needs to different teams.
