Clinical Quality Assurance Manager

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

Job summary

A leading global diagnostics organization is seeking a Clinical Quality Assurance Manager for a 12-month contract in Greater Manchester. The role involves overseeing quality and compliance in clinical trials, providing leadership, and ensuring regulatory adherence. This position offers a chance to contribute to impactful clinical programs in a dynamic environment.

Qualifications

• Proven background in quality within a Clinical environment.
• Qualified Auditor with knowledge of GCP.

Responsibilities

• Oversee quality and compliance across global clinical trial activities.
• Manage workload and offer expert guidance to the Clinical QA team.
• Participate in internal audits and act as a Subject Matter Expert.

Skills

Leadership

Compliance

Quality Assurance

Auditing

Education

Degree in a relevant discipline

Job description

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About

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 continuous innovation 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 oversee quality and compliance across global clinical trial activities, supporting high-quality, regulatory-compliant diagnostic studies.

Key Responsibilities

1. Provide leadership and support to the Clinical QA team, managing workload and offering expert guidance.
2. Collaborate with the Clinical Affairs team to maintain trial compliance, addressing deviations and complaints.
3. Review trial documentation and Clinical Affairs SOPs to ensure ongoing compliance.
4. Contribute to the reporting of Clinical Affairs compliance metrics.
5. Participate in internal audits and act as a Subject Matter Expert during inspections and audits.

Requirements

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

Why Apply?

Join a dynamic, entrepreneurial organization that values innovation and collaboration. This role offers a chance to contribute to impactful clinical programs and advance your career in an inclusive, growth-oriented environment.

Additional Information

• Work experience in QA.
• Languages: English.
• Seniority level: Mid-Senior level.
• Employment type: Contract.
• Industries: Technology, Information and Internet.