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Position: Principal Research Fellow - Clinical Trials group manager/Lead
Institution: University College London
Department: CRUK & UCL Cancer Trials Centre
Location: London, United Kingdom
Duties: The Clinical Trials Manager (Trials Group Lead, TGL) is classified as a senior post at UCL (Principal Research Fellow). This post will lead a team of Senior Trial Coordinators (STC), Trial Coordinators, Database Developers, Data Managers and Trials Assistants, and will take responsibility for the timely and orderly development and delivery of a portfolio of trials. Currently, the post covers trials involving Advanced Therapies, especially gene and cell therapies. The post holder will be responsible for managing their team and portfolio of trials in order to make the most efficient use of resources available. He/she will work with clinical and scientific experts in these cancer types
Requirements: The postholder will have a University degree, or nursing qualification, along with a postgraduate qualification and/or evidence of publications. He/she should have considerable recent experience in clinical trials and their conduct, with experience of managing a portfolio of trials, and knowledge of trial design and conduct, particularly in conducting clinical trials involving investigational medicinal products (licensed or unlicensed); An in-depth knowledge of regulations and guidelines governing the conduct of CTIMP clinical trials in the UK (and EU), and experience of working to these (including pharmacovigilance and contract manufacture) is essential
   
Text: Principal Research Fellow - Clinical Trials group manager/Lead, - Ref:1873989 Click here to go back to search results Apply Now UCL Department / Division CRUK & UCL Cancer Trials Centre Location of position London Grade 9 Hours Full Time (Job share considered) Salary (inclusive of London allowance) £57,342 - £62,346 per annum Duties and Responsibilities The Clinical Trials Manager (Trials Group Lead, TGL) is classified as a senior post at UCL (Principal Research Fellow). This post will lead a team of Senior Trial Coordinators (STC), Trial Coordinators, Database Developers, Data Managers and Trials Assistants, and will take responsibility for the timely and orderly development and delivery of a portfolio of trials. Currently, the post covers trials involving Advanced Therapies, especially gene and cell therapies . The post holder will be responsible for managing their team and portfolio of trials in order to make the most efficient use of resources available. He/she will work with clinical and scientific experts in these cancer types. Trial Group leadership will also involve project management, scientific input into new trials and collaborating with national scientific bodies to acquire new trials whilst making best use of CTC resources and capacity. The post holder will be part of the Senior Management Group, the remit of which is to oversee the function of the CTC and to ensure the strategic aims of the CTC are in line with local and national policies and initiatives. The TGL is a multi-faceted role and will require interaction with many different groups and individuals within the CTC (including finance, administration, statistics and regulatory) and national bodies such as Cancer Research UK, NCRI, UKCRN, NIHR, MHRA, HRA and international groups, as appropriate. As a senior member of the department the TGL will be expected to share additional responsibilities that arise within the CTC, both internally and externally. We welcome applications from those looking to work on a part time basis, ideally a minimum of 0.5 FTE (18.25 hours per week). Applicants should state their FTE preference on the application form. Duration of the post is grant funded until September 2023, in the first instance. Key Requirements The postholder will have a University degree, or nursing qualification, along with a postgraduate qualification and/or evidence of publications. He/she should have considerable recent experience in clinical trials and their conduct, with experience of managing a portfolio of trials, and knowledge of trial design and conduct, particularly in conducting clinical trials involving investigational medicinal products (licensed or unlicensed). An in-depth knowledge of regulations and guidelines governing the conduct of CTIMP clinical trials in the UK (and EU), and experience of working to these (including pharmacovigilance and contract manufacture) is essential. Further Details A job description and person specification can be accessed at the bottom of this page. To apply for the vacancy please click on the Apply Now button below. If you have any queries regarding the vacancy or application process, please contact ctc.hr@ucl.ac.uk. We particularly welcome female applicants and those from an ethnic minority, 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 31 Jan 2021 Latest time for the submission of applications 23:59 Interview date TBC Our department holds an Athena SWAN Silver award, in recognition of our commitment and demonstrable impact in advancing gender equality. 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 specification Apply Now
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