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Clinical Quality Assurance Manager

Cpl Life Sciences
Posted 23 days ago, valid for 7 days
Location

Manchester, Greater Manchester M17 1DJ, England

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 Clinical Quality Assurance Manager position is a 12-month fixed-term contract based in Manchester, UK, requiring 3 days on-site each week.
  • The role offers a salary ranging from £40,000 to £46,000, along with a 10% bonus.
  • Candidates must have a minimum of 5 years of experience in a GCP environment and a degree-level qualification or equivalent experience.
  • Key responsibilities include overseeing the Clinical QA team, ensuring compliance during trial activities, and participating in the Internal Audit program.
  • This hybrid role does not offer sponsorship and requires candidates to have the full right to work in the UK.

Job Title: Clinical Quality Assurance Manager  

Job Type: 12 months fixed-term contract, Maternity cover

Location: Manchester, UK (hybrid) 3x a week on site

Remuneration: £40,000 - £46,000 + 10% Bonus

Cpl Life Sciences is partnering with a leading organisation that use technologies to help customers extract, analyze, and interpret molecular data from samples containing DNA, RNA, and proteins.

Due to maternity leave, we are looking for an experienced candidate to take responsibility for quality and compliance oversight of the activities performed by the Clinical Affairs team. The function supports the testing and registration of diagnostic tests/ instruments covering a diverse portfolio of indications. The scope of the trials is global and includes multi-centre trials managed out of several different locations.

Key responsibilities:

·      As a senior member of the Clinical QA team, take responsibility for overseeing division of workload, advising, and supporting the team as required

·       Work with members of the Clinical Affairs team to ensure compliance during trial activities e.g. closure of deviations, complaints etc.

·      Review Clinical relevant documentation throughout the clinical trial

·      Coordinate and provide input to reporting of Clinical Affairs compliance KPIs

·      Participate in the Internal Audit program

·      Review Clinical Affairs SOPs

Position Requirements:

·      Degree-level qualification (or equivalent experience)

·      Minimum 5 years’ experience in a GCP environment with demonstrable, working knowledge of GCP practices

·      Desirable: working knowledge of IVD or medical device regulations

·      Qualified Auditor

·      Experience in performing as a Subject Matter Expert in regulatory inspections and other formal audits

·      Willingness to travel internationally up to 10%

·      A strong team player with excellent communication and interpersonal skills who puts value into working cross functionally with multinational/ cultural teams and individuals

This role will be a hybrid-based position with 3x a week required on site in Manchester. Please note this role does not offer sponsorship and will need candidates to hold the full right to work in the UK.

For more information, please contact me at

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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.