Clinical Trials Quality Assurance Specialist
4 weeks ago
About the Role:
The Medicines Evaluation Unit Ltd is seeking a skilled Clinical Trials Quality Assurance Specialist to join our team. In this role, you will play a key part in overseeing our quality systems, reviewing quality documentation, and managing deviations, change controls, and CAPAs (Corrective and Preventive Actions). You will also conduct internal and vendor audits in accordance with the approved audit programme and host sponsor audits and regulatory inspections as required.
Your Key Responsibilities:
- Conducting internal and vendor audits in accordance with the approved audit programme.
- Hosting sponsor audits and regulatory inspections, as required.
- Maintaining and improving the quality systems to ensure full compliance.
- Writing clear and concise reports and communicating effectively with colleagues, vendors, and regulators.
What We Offer:
- Starting salary dependent on experience.
- Immediate start.
- Continuous professional development opportunities.
- 29 days annual leave.
- Company pension scheme.
- Generous annual bonus.
- Healthcare plan.
- Free parking.
Requirements:
- Enthusiastic, self-motivated, and highly organized.
- Experienced in working in a quality role within a clinical trial organization.
- Proficient in Microsoft Office.
- A good communicator with strong attention to detail.
- A science background is advantageous but not essential.
- A full UK driving licence is required, as the role involves travel between sites.
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