Clinical QA Manager - Interim
| Job Type | Temporary / Contract |
| Location | London |
| Area | Central London, UK |
| Sector | Clinical Research |
| Salary | £0 per year |
| Currency | gbp |
| Start Date | ASAP |
| Advertiser | remoteapi |
| Job Ref | 1503 |
| Job Views | 3 |
- Description
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
Qualifications and Experience
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
#QA
- Strong years of experience in clinical research, including time spent in Quality Assurance and Compliance within a CRO, pharmaceutical or biotech environment
