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Position: Trial Manager
Institution: University College London
Department: Institute of Clinical Trials & Methodology
Location: London, United Kingdom
Duties: The Trial Manager will be responsible for the day to day co-ordination of this clinical trial of an advanced therapy investigational medicinal product (ATIMP) working closely with the other members of the team and the sites to ensure the successful delivery of the trial. The main duties of the post include training the site staff on the trial procedures, writing documentation, monitoring the data and ensuring that all regulatory requirements are met in a timely manner
Requirements: The post would suit an individual with experience in the coordination of a complex clinical trial of an IMP and an excellent knowledge of current regulatory requirements governing clinical trials including a practical understanding of GCP. We are looking for someone with good scientific and clinical trial knowledge and on-site monitoring experience. Successful applicants will have excellent organisational and excellent written and verbal communication skills as well as good attention to detail. Applicants should have the ability to work as part of a team and independently
   
Text: Trial Manager, - Ref:1622027 Click here to go back to search results Apply Now UCL Department / Division Institute of Clinical Trials & Methodology Specific unit / Sub department Comprehensive Clinical Trials Unit Grade 7 Hours Part Time Hours per week (%FTE) 18.25 hours per weeks (50% FTE) Salary (inclusive of London allowance) ?34,056- ?41,163 per annum Salary pro-rata for part time vacancies Duties and Responsibilities The Comprehensive Clinical Trials Unit at UCL (CCTU) collaborates with researchers to design, conduct, analyse and publish clinical trials and other well-designed studies. The CCTU provides clinical, statistical and trial operations leadership. This appointment is funded for 6 months. The Trial Manager will be responsible for the day to day co-ordination of this clinical trial of an advanced therapy investigational medicinal product (ATIMP) working closely with the other members of the team and the sites to ensure the successful delivery of the trial. The main duties of the post include training the site staff on the trial procedures, writing documentation, monitoring the data and ensuring that all regulatory requirements are met in a timely manner. Key Requirements The post would suit an individual with experience in the coordination of a complex clinical trial of an IMP and an excellent knowledge of current regulatory requirements governing clinical trials including a practical understanding of GCP. We are looking for someone with good scientific and clinical trial knowledge and on-site monitoring experience. Successful applicants will have excellent organisational and excellent written and verbal communication skills as well as good attention to detail. Applicants should have the ability to work as part of a team and independently. Experience of managing an ATIMP would be advantageous. 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 the application process, please contact Thowani Lungu ( t.lungu@ucl.ac.uk ), ( 44 20 3549 5018). We particularly welcome applications from black and minority ethnic candidates as they are under-represented within UCL at this level. Closing Date 26 Jan 2017 Latest time for the submission of applications 11:59 Interview date TBC Our department holds an Athena SWAN Bronze award, which illustrates our commitment to addressing 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 the UCL Terms and Conditions related to this job, employee benefits that we offer and further information about UCL . Job Description & Person Specification Apply Now
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