R&D Clinical Co-op

Stryker Corporation; Belfast; On-site; GBP 20,000 - 25,000; Full time

Job summary

A leading medical technology company is seeking an R&D Clinical Co-op in Belfast, UK. This full-time position involves supporting pre-clinical and clinical testing, assisting in data management, and contributing to regulatory documentation. Ideal candidates will have an ongoing degree in a relevant field and strong communication skills. Familiarity with cardiovascular devices is a plus.

Qualifications

• Understanding of cardiovascular anatomy and physiology.
• Knowledge of medical devices, particularly cardiovascular.
• Experience with general electronics hardware is beneficial.

Responsibilities

• Support pre-clinical, clinical, and usability testing activities.
• Assist in data management and analysis of clinical data.
• Help with engineering documentation for clinical regulatory submissions.

Skills

Excellent communication skills

Problem solving and analytical skills

Technical writing skills

Time management skills

Good teamwork skills

Education

Relevant ongoing degree course

Relevant A-levels or equivalent

Tools

Microsoft Office

MS Project

Adobe Acrobat

Job description

R&D Clinical Co-op page is loaded## R&D Clinical Co-oplocations: Belfast, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R549614Work Flexibility: Not availableProvide 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 marketing1. Supporting post-market clinical follow up activities2. Assist data management of clinical and pre-clinical data including the creation of data management plans3. Assist in execution of pre-clinical studies4. Assist data processing activities5. Assist in data recording during usability and pre-clinical studies6. Assist with engineering documentation for clinical regulatory submissions and pre-submissions7. Assist in initial Bench/Pilot testing and writing or review of technical reports8. Assist in planning pre-clinical and usability studies including equipment sourcing and preparation of data recording templates9. Liaising with the training officer and assisting in the training of industrial placement students;10. Assist in the preparation and organisation of stakeholder and advisory meetings.11. Creating and updating documentation in accordance with ISO 13485, GLP and ISO 14155• Qualifications: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 useful• System/Computer Requirements:Basic Microsoft Office, MS Project, Adobe AcrobatAbility to utilise publication search engines.• Key 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 initiativeTravel Percentage: None