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Job Location | Bynea |
Education | Not Mentioned |
Salary | £30,000 - £35,000 per annum |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent , full-time |
The Recruitment Co are recruiting an experienced Clinical Trials Software Support Engineer to join our clients expanding team. A world-leading manufacturer of high-quality technical products.Contract: Permanent Salary: Up to £35,000p.a Shifts: Full time DaysThe Role/Responsibilities: Our client is looking for a multi-skilled Software Engineer to support in the ongoing clinical trials undertaken to prove the safety and efficacy of products developed by the company.Our client undertakes numerous clinical trials in-house and the company has developed bespoke software to facilitate this function. This software is used to manage each individual appointment, provide step-by-step guidance on the procedures to be followed alongwith real-time data collection at each step, the data being either captured visual images, physiological measurements via interfaced devices or questionnaire responses. All the data gathered is stored in a highly regimented format and structure to ensure accuracyand repeatability across each study. The successful candidate will be responsible for maintaining and improving the existing system, providing day-to-day support and ensuring optimal performance and data integrity across numerous clinical suites.The company has also developed complex image analysis tools that allow quantification of key metrics such as hair counts pre and post treatment. These automated tools are utilised to determine the efficacy of the Companies products using high resolution imagescaptured during the clinical studies. You will be responsible for maintaining, supporting and improving the existing system with a particular focus on ensuring accuracy and integrity of the data.In addition to direct support of the clinical department, you will be involved in the development of document management systems for the entire business. As the company operates according to numerous International Regulatory Standards, i.e., EU Medical DeviceDirective and the USA FDA, accurate document control is vital to the ongoing function of the business. The successful candidate will be heavily involved in the development of a business-wide document management system that captures inputs from design/development/clinical/regulatory and manufacturing departments.Software/Hardware - Essential Requirements Windows forms applications in VB/C#/.NET including: