Work Flexibility: Not available
Provide support for pre-clinical clinical and usability testing activities within the clinical dept. The team member will provide support in document management data management and analysis. The team member will also support other functions such as regulatory quality and post-market clinical follow up data management of clinical and pre-clinical data including the creation of data management in execution of pre-clinical data processing in data recording during usability and pre-clinical with engineering documentation for clinical regulatory submissions and in initial Bench/Pilot testing and writing or review of technical reports in planning pre-clinical and usability studies including equipment sourcing and preparation of data recording with the training officer and assisting in the training of industrial placement students; in the preparation and organisation of stakeholder and advisory and updating documentation in accordance with ISO 13485 GLP and ISO 14155Qualifications:Relevant on-going degree course with acceptable 1st year resultsRelevant A-levels of equivalent Specific Knowledge:Knowledge and understanding of cardiovascular anatomy and physiologyKnowledge of medical devices particularly cardiovascularKnowledge or experience of general electronics hardware would be usefulSystem/Computer Requirements:Basic Microsoft Office MS Project Adobe AcrobatAbility to utilise publication search Competencies needed for this position:Excellent communication skills (both written and verbal)Problem solving and analytical skillsTechnical writing skillsTime management skillsHigh standard of work and strong attention to detailGood teamwork skills and ability to work as part of a multi-disciplinary teamAbility to work under pressure against tight deadlinesDemonstrate initiative
Travel Percentage: None