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Research Nurse

Job in City of Edinburgh, Edinburgh, City of Edinburgh Area, EH1, Scotland, UK
Listing for: University of Edinburgh
Full Time, Part Time, Contract position
Listed on 2026-01-20
Job specializations:
  • Healthcare
  • Research/Development
Salary/Wage Range or Industry Benchmark: 34610 - 39906 GBP Yearly GBP 34610.00 39906.00 YEAR
Job Description & How to Apply Below
Position: 13460- Research Nurse
Location: City of Edinburgh

Grade UE07: £34,610- £39,906 per annum (pro rata)

CMVM, School of Regeneration and Repair

Full Time: 35 hours per week for first 3 months, reducing to 17.5 hours for further 9 months

Fixed Term: 12 months

The Opportunity

To work as part of a team who are researching ways to improve the success of in vitro fertilisation (IVF).

We are looking for a clinical research nurse to participate in an exciting research project aimed at understanding the molecular origins of abnormalities in human oocytes and embryos.

Please note that this vacancy will be full-time for the first 3 months and then will reduce to 17.5 hours per week for the further 9 months. However, we are open to considering part-time or flexible working patterns.

The salary for this post is £34,610 to £39,706 per annum.

Responsibilities
  • Participate in the IVF research project, contributing to the investigation of molecular origins of abnormalities in human oocytes and embryos.
  • Conduct patient identification and recruitment for clinical research studies.
  • Obtain informed patient consent for diverse clinical research studies.
  • Manage research data and databases, ensuring accurate and secure record‑keeping.
  • Adhere to ICH GCP Guidelines, EU Clinical Trials Directive, and Research Governance Framework throughout project activities.
Your skills and attributes for success
  • First level registered nurse with relevant experience demonstrating the appropriate competencies and skills (particularly communication, organisation) for the job.
  • Experience/knowledge of ethics and R&D applications is desirable.
  • Evidence of further education including post‑graduate certification/diploma/Continuous Professional Development in a relevant area.
  • Previous experience of conducting patient identification and recruitment; obtaining informed patient consent for clinical research studies of a diverse nature is desirable but not essential. Relevant research experience includes awareness of ICH GCP Guidelines, EU Clinical Trials Directive and Research Governance Framework.
  • Experience with database management and working knowledge of appropriate IT skills is essential.
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