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- Tasks: Lead quality and compliance initiatives in clinical research projects.
- Company: Dynamic client in Central London focused on innovation in healthcare.
- Benefits: Competitive contract rate, flexible working arrangements, and professional development opportunities.
- Other info: Join a collaborative team dedicated to continuous improvement and quality culture.
- Why this job: Make a real impact on quality standards in the clinical research field.
- Qualifications: Experience in clinical QA, compliance, and regulatory requirements essential.
The predicted salary is between 46000 - 52000 £ per year.
We are looking for a contract QA Manager to work with a client in Central London. We need a QA & Compliance Manager to lead and continuously strengthen quality and compliance framework across all project activities. This role is responsible for the hands-on implementation and oversight of the Quality Management System, ensuring compliance with applicable regulatory requirements, industry standards and client expectations.
The QA & Compliance Manager will provide practical guidance to study teams, proactively manage risk, oversee audits and inspections and drive continuous improvement across the business. Acting as a key partner to operational teams and senior leadership, the role plays a critical part in maintaining inspection readiness, supporting business growth and embedding a strong quality culture throughout.
Key Responsibilities:- Quality Management System (QMS)
- Risk Management & Oversight
- Quality Assurance & Compliance
- Audits, Inspections & Continuous Improvement
- Training & Quality Culture
- Regulatory Intelligence & Reporting
- Data Protection & Governance
- Vendor & Partner Oversight
Ideal background:
- Strong years of experience in clinical research, including time spent in Quality Assurance and Compliance within a CRO, pharmaceutical or biotech environment
- Demonstrated experience developing, implementing and maintaining a Quality Management System (QMS) in a regulated clinical research setting
- Strong working knowledge of ICH-GCP, ISO standards and applicable global regulatory requirements
- Proven experience managing clinical audits, vendor audits and regulatory inspections
- Hands-on experience investigating quality issues, deviations and non-conformances, including leading root cause analysis and CAPA development
- Experience assessing and managing compliance risks related to new services, technologies or business initiatives
- Demonstrated experience providing QA guidance and oversight to cross-functional clinical teams
- Prior experience acting as, or supporting, a Data Protection Officer (DPO) role and ensuring compliance with data protection legislation (e.g. GDPR) preferred
- Experience developing and delivering quality and compliance training programs
Clinical QA Manager - Interim in London employer: Pop Science
Contact Detail:
Pop Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical QA Manager - Interim in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP and ISO standards. Be ready to discuss how you've implemented quality management systems in the past, as this will show you're the right fit for the QA Manager role.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and expertise. Check out our website for openings that match your skills, especially in QA and compliance within clinical settings.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Mention something specific from your conversation to show your genuine interest in the role.
We think you need these skills to ace Clinical QA Manager - Interim in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical QA Manager role. Highlight your experience in quality assurance and compliance, especially in clinical research. We want to see how your background aligns with the job description!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Mention specific experiences that demonstrate your ability to lead quality management systems and manage compliance risks.
Showcase Relevant Skills: Don’t forget to showcase your skills related to ICH-GCP, ISO standards, and regulatory requirements. We’re looking for someone who can hit the ground running, so make sure these skills stand out in your application.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss any important updates from us!
How to prepare for a job interview at Pop Science
✨Know Your QMS Inside Out
Make sure you have a solid understanding of Quality Management Systems, especially in a clinical research context. Be ready to discuss your experience with developing and maintaining a QMS, as well as how you've ensured compliance with regulatory requirements.
✨Showcase Your Audit Experience
Prepare specific examples of audits you've managed or participated in. Highlight your role in these processes and any improvements you implemented as a result. This will demonstrate your hands-on experience and ability to drive continuous improvement.
✨Understand Risk Management
Be prepared to talk about how you've assessed and managed compliance risks in previous roles. Share examples of how you've proactively identified potential issues and the steps you took to mitigate them.
✨Emphasise Your Training Skills
Since training is a key part of this role, think about how you've developed and delivered quality and compliance training programs in the past. Discuss your approach to fostering a strong quality culture within teams and how you ensure everyone is inspection-ready.