Clinical Quality Assurance Manager

ZipRecruiter; Manchester; On-site; GBP 46,000; Full time

Job summary

Join a pioneering global diagnostics organization as a Clinical Quality Assurance Manager in Greater Manchester. This 12-month contract role offers a unique opportunity to lead quality and compliance in clinical trials, ensuring high standards in regulatory-compliant diagnostic studies. You'll work in a dynamic environment that values innovation and collaboration, contributing to impactful clinical programs. If you're a proactive QA professional looking to advance your career while making a difference in healthcare, this position is for you.

Qualifications

• Proven background in quality within a clinical environment.
• Qualified Auditor with knowledge of GCP and IVD regulations.

Responsibilities

• Lead and support the Clinical QA team, ensuring compliance.
• Collaborate with Clinical Affairs to maintain trial compliance.

Skills

Leadership

Quality Assurance

Regulatory Compliance

Clinical Trial Management

Auditing

GCP Knowledge

Education

Degree in a relevant discipline

Job description

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 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:

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 issues such as deviations and complaints.
3. Review trial documentation and Clinical Affairs SOPs to ensure ongoing compliance.
4. Contribute to the reporting of key Clinical Affairs compliance metrics.
5. 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.