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Clinical Quality Assurance Manager

SRG
Posted 16 hours ago, valid for a month
Location

Manchester, Greater Manchester M24WU, England

Salary

£46,000 per annum

Contract type

Full Time

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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 an experienced Clinical QA professional to oversee quality and compliance across global clinical trial activities.
  • Candidates should possess a degree (or equivalent experience) in a relevant discipline and have a proven background in quality within a clinical environment.
  • A Qualified Auditor with knowledge of GCP and experience with IVD or medical device regulations is highly desirable, along with flexibility for international travel up to 10%.
  • This opportunity allows for significant contributions to 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.

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