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Position: Quality Assurance Officer/Documents Manager
Institution: University College London
Department: Cancer Institute
Location: London, United Kingdom
Duties: 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
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
   
Text: Quality Assurance Officer / Documents Manager, - Ref:1776967 Click here to go back to search results Apply Now UCL Department / Division Cancer Institute Specific unit / Sub department Cancer Research UK & UCL Cancer Trials Centre Location of position London Grade 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. Further Details To apply please click the "apply now" button below. A full job description is accessible at the bottom of this page. If you have any queries regarding the vacancy, please contact Roisin Beehag, r.beehag@ucl.ac.uk , 020 7976 9859. For all queries regarding the application process, please contact Louise Rusha, l.rusha@ucl.ac.uk , 0207 679 9898. We particularly welcome applications from black and minority ethnic candidates as they are under-represented within UCL at this level. We will consider applications to work on a part-time, flexible and job share basis wherever possible. Closing Date 28 Dec 2018 Latest time for the submission of applications 23.59 Interview date 14 January 2019 Our department holds an Athena SWAN Silver award, in recognition of our commitment and demonstrable impact in advancing gender equality. This role does not meet the eligibility requirements for a tier 2 certificate of sponsorship under UK Visas and Immigration legislation. Therefore UCL will not be able to sponsor individuals who require right to work in the UK to carry out this role. This appointment is subject to UCL Terms and Conditions of Service for Research and Support Staff. Please use these links to find out more about UCL working life including the benefits we offer and UCL Terms and Conditions related to this job. Job description and person spec Apply Now
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