Clinical Quality Assurance Manager

SRG; Manchester; On-site; GBP 46,000 - 53,000; Full time

Job summary

A leading global diagnostics organisation in Greater Manchester seeks an experienced Clinical Quality Assurance Manager for a 12-month contract. You will oversee quality and compliance across global clinical trial activities and provide leadership to a dynamic Clinical QA team. Ideal candidates will have a degree in a relevant discipline and a proven background in quality in clinical environments. This is a unique chance to contribute to impactful clinical programs and advance your career in a growth-focused environment.

Qualifications

• Proven background within quality in a Clinical environment.
• Qualified Auditor with demonstrable knowledge of GCP.
• Experience with IVD or medical device regulations highly desirable.

Responsibilities

• Oversee quality and compliance across global clinical trial activities.
• Provide leadership and support to the Clinical QA team.
• Collaborate with the Clinical Affairs team to maintain trial compliance.
• Participate in internal audits and act as Subject Matter Expert.

Skills

Leadership and support

Quality compliance

Knowledge of GCP

Problem-solving

Education

Degree in relevant discipline

Job description

Clinical Quality Assurance Manager

£46,000 - 12-month contract

Greater Manchester

SRG are proud to be working on behalf of a leading global diagnostics organisation, currently seeking an experienced Clinical Quality Assurance Manager to join their team in Greater Manchester.

Our client is a pioneering force in science and healthcare. Improving lives across the world, through their continuous innovation, developing and delivering life-changing diagnostic solutions.

The Role:
This is a 12-month contract position ideal for a proactive and knowledgeable Clinical QA professional. You will take a senior role in overseeing quality and compliance across global clinical trial activities, supporting the delivery of high-quality, regulatory-compliant diagnostic studies.

Key Responsibilities:

• Provide leadership and support to the Clinical QA team, managing workload and offering expert guidance
• Collaborate with the Clinical Affairs team to maintain trial compliance, addressing issues such as deviations and complaints
• Review trial documentation and Clinical Affairs SOPs to ensure ongoing compliance
• Contribute to the reporting of key Clinical Affairs compliance metrics
• Participate in the internal audit programme and act as a Subject Matter Expert during inspections and audits

Requirements:

• Degree (or equivalent experience) in a relevant discipline
• Proven background within quality in a Clinical environment.
• Qualified Auditor with demonstrable knowledge of GCP
• Experience working with IVD or medical device regulations is highly desirable
• Flexibility to travel internationally (up to 10%)

Why Apply?

You'll be joining a dynamic, entrepreneurial organisation that values innovation, collaboration, and the opportunity to make a real difference. This is a unique chance to contribute to globally impactful clinical programs and advance your career in an inclusive, growth-focused environment.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.