QA Vacancies
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We have 2 Quality Assurance Officer / Documents Manager vacancies being advertised at the CR UK & UCL Cancer Trials Centre.
Quality Assurance Officer / Documents Manager (Grade 6)
Cancer Research UK & UCL Cancer Trials Centre, London
Grade: UCL 6
Hours: Full Time
Salary (inclusive of London allowance): £28,574 – £33,487 per annum
Duties and Responsibilities
The Cancer Research UK & UCL Cancer Trials Centre (CTC) is part of the Cancer Institute at University College London and is based on Tottenham Court Road. The majority of staff are funded on Cancer Research UK programme or project grants and there is some additional support in the form of educational grants from industry.
The postholder will be a member of the CTC Regulatory team, a group which supports and advises CTC trial staff to ensure compliance with applicable guidelines and regulations. The 6 members of the team have expertise in the areas of: quality assurance, audit, sponsor authorisations and oversight, contracts and pharmacovigilance.
The main purpose of the QA Officer role is to manage the day-to-day running, maintenance and improvement of the CTC quality system, and in particular management of centrally controlled/maintained documents and templates.
The role holder will be responsible for maintaining a portfolio of central standard operating procedures (SOPs) at the CTC, including arranging/providing staff training relating to the procedures and related templates. He/she will be required to follow through allocated activities and projects to completion, and to provide updates to relevant members of the Regulatory team and other CTC staff, as required.
The post is funded for 1 year in the first instance.
Key Requirements
The post would suit proactive, enthusiastic individual interested in developing skills in quality assurance, audit and other areas, within a clinical trials environment.
The postholder will have a comprehensive knowledge of life sciences and will be able to provide evidence of working to, and an understanding of, relevant current clinical trial and research regulations (in particular the EU Clinical Trials and GCP Directives, the Medicines for Human Use (Clinical Trials) Regulations and the UK Policy Framework for Health and Social Care Research). Familiarity with SOPs and document version control is essential and a knowledge of cancer would be advantageous.
Closing date: 28 December 2018
Click here for further details and to apply https://atsv7.wcn.co.uk/search_engine/jobs.cgi?SID=amNvZGU9MTc3Njk2NyZ2dF90ZW1wbGF0ZT05NjUmb3duZXI9NTA0MTE3OCZvd25lcnR5cGU9ZmFpciZicmFuZF9pZD0wJnBvc3RpbmdfY29kZT0yMjQ=
Quality Assurance Officer / Documents Manager (Grade 7)
Cancer Research UK & UCL Cancer Trials Centre, London
Grade: UCL 7
Hours: Full Time
Salary (inclusive of London allowance): £35,328 – £42,701 per annum
Duties and Responsibilities
The Cancer Research UK & UCL Cancer Trials Centre (CTC) is part of the Cancer Institute at University College London and is based on Tottenham Court Road. The majority of staff are funded on Cancer Research UK programme or project grants and there is some additional support in the form of educational grants from industry.
The postholder will be a member of the CTC Regulatory team, a group which supports and advises CTC trial staff to ensure compliance with applicable guidelines and regulations. The 6 members of the team have expertise in the areas of: quality assurance, audit, sponsor authorisations and oversight, contracts and pharmacovigilance.
The main purpose of the QA Officer role is to manage the day-to-day running, maintenance and improvement of the CTC quality system, and in particular management of centrally controlled/maintained documents and templates.
The role holder will be responsible for maintaining a portfolio of central standard operating procedures (SOPs) at the CTC, including arranging/providing staff training relating to the procedures and related templates. He/she will be required to follow through allocated activities and projects to completion, and to provide updates to relevant members of the Regulatory team and other CTC staff, as required.
The post is funded for 1 year in the first instance.
Key Requirements
The post would suit proactive, enthusiastic individual interested in developing skills in quality assurance, audit and other areas, within a clinical trials environment.
The postholder will have a comprehensive knowledge of life sciences and will be able to provide evidence of working to, and an understanding of, relevant current clinical trial and research regulations (in particular the EU Clinical Trials and GCP Directives, the Medicines for Human Use (Clinical Trials) Regulations and the UK Policy Framework for Health and Social Care Research). The postholder will have experience of conducting clinical trials and/or clinical research studies, writing SOPs, work instructions or policies, familiarity with the audit process (preferably with experience of conducting audits) and significant experience of report writing in lay and scientific language. Previous experience of working in a clinical trials unit would be advantageous.
Closing date: 28 December 2018
Click here for further details and to apply https://atsv7.wcn.co.uk/search_engine/jobs.cgi?SID=amNvZGU9MTc3Njk3MSZ2dF90ZW1wbGF0ZT05NjUmb3duZXI9NTA0MTE3OCZvd25lcnR5cGU9ZmFpciZicmFuZF9pZD0wJnBvc3RpbmdfY29kZT0yMjQ=
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