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Clinical Quality Assurance Manager

SRG
Posted 16 hours ago, valid for a month
Location

Manchester, Greater Manchester M17 1DJ, England

Salary

£46,000 - £12 per month

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The position is for a Clinical Quality Assurance Manager on a 12-month contract in Greater Manchester, offering a salary of £46,000.
  • The role requires a proactive and knowledgeable Clinical QA professional with a proven background in quality within a clinical environment.
  • Candidates must possess a degree or equivalent experience, along with qualifications as an auditor and knowledge of GCP.
  • Experience with IVD or medical device regulations is highly desirable, and flexibility to travel internationally (up to 10%) is required.
  • This opportunity allows for significant contributions to globally impactful clinical programs within a dynamic and innovative organization.

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.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.