Senior Research Officer in Clinical Trials Management
Listed on 2026-06-23
-
Research/Development
Research Scientist
Senior Research Officer in Clinical Trials Management
Job Number SU01617
Contract Type:
Fixed Term
Salary: £46,735 to £55,755 per annum
Working Pattern:
Full Time
Faculty/Directorate:
Faculty of Medicine, Health and Life Science
Location:
Singleton Campus, Swansea
Closing Date: 5 Jul 2026
Interview Date: 22 Jul 2026
Informal Enquiries:
- Deborah Fitzsimmons
- Kym Carter
The post holder will set up and manage research projects that include Clinical Trials of Investigational Medicinal Products (CTIMPs) on the Swansea Trials Unit portfolio. This involves developing and managing key documentation for the projects such as protocols, participant information sheets and consent forms, trial management plans and reports. The role requires close collaboration with STU data managers and statisticians to facilitate accurate data collection and analysis, and with a multi‑organisational project team to ensure that projects are delivered on time and to a high standard.
Additional responsibilities include supporting departmental staff with their research projects and contributing to research funding applications.
The University is committed to supporting and promoting equality and diversity in all its practices and activities. We welcome diverse applications from protected characteristics including age, disability, gender reassignment, marriage and civil partnership, pregnancy and maternity, race (including colour, nationality, ethnic and national origin), religion or belief, sex, and sexual orientation.
Welsh Language SkillsLevel 1 – A little. The role holder should be able to pronounce Welsh words, answer the phone in Welsh, and use very basic everyday words and phrases. Level 1 can be achieved by completing a 1‑hour course.
Additional InformationApplicants must submit a CV and cover letter. Short‑listed candidates will be invited to interview, which will include a 5‑minute presentation responding to: "What will be your strategy and plan to deliver a clinical trial of a CTIMP to meet the standards required of a UK registered clinical trials unit?"
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