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- Tasks: Lead quality assurance and compliance in clinical research projects.
- Company: Dynamic client in Central London focused on innovation.
- Benefits: Competitive contract rate, flexible working environment, and professional growth opportunities.
- Why this job: Make a real impact on quality culture and compliance in the healthcare sector.
- Qualifications: Experience in clinical research and strong knowledge of regulatory standards required.
- Other info: Join a collaborative team dedicated to continuous improvement and excellence.
The predicted salary is between 50000 - 60000 £ 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)
- Quality Assurance & Compliance
- Audits, Inspections & Continuous Improvement
- Training & Quality Culture
- Regulatory Intelligence & Reporting
- Data Protection & Governance
- 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: Coronado Research
Contact Detail:
Coronado Research 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 roles.
✨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 our needs!
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. Share specific examples of your experience with QMS and audits, and show us your passion for maintaining high-quality standards.
Showcase Your Regulatory Knowledge: Since this role involves ensuring compliance with regulatory requirements, make sure to mention your knowledge of ICH-GCP and ISO standards. We love seeing candidates who are up-to-date with industry regulations!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, we love seeing candidates who follow our process!
How to prepare for a job interview at Coronado Research
✨Know Your QMS Inside Out
Make sure you’re well-versed in Quality Management Systems, especially how they apply to clinical research. Be ready to discuss your experience with developing and maintaining a QMS, as this will show your hands-on expertise and understanding of regulatory requirements.
✨Showcase Your Audit Experience
Prepare specific examples of audits you've managed or participated in. Highlight any challenges you faced and how you overcame them. This will demonstrate your ability to handle inspections and maintain compliance, which is crucial for the role.
✨Emphasise Continuous Improvement
Think about instances where you’ve driven continuous improvement in quality processes. Be ready to share how you’ve implemented changes based on audit findings or compliance issues, showcasing your proactive approach to risk management.
✨Be Ready for Scenario Questions
Expect scenario-based questions that test your problem-solving skills in real-world situations. Prepare to discuss how you would handle specific compliance risks or quality issues, as this will reflect your practical guidance capabilities to study teams.