Clinical Conduct Associate (Medical Research)
Celerion
Belfast, Northern IrelandView on map(opens Google Maps in a new tab)
Salary
£28,000
Contract
Not specified
Hours
Full time
Closing date
Not specified
In plain English
What this job actually involves
The role helps run early‑phase drug studies, supporting participants and collecting data. It suits people who like science, teamwork and careful work.
What you'll need
- Interest in medical research or health science
- Good communication and listening skills
- Attention to detail and ability to follow procedures
- Basic computer skills for data entry
- Ability to work well in a team
How to boost your chances
- Read up on clinical trial basics and GCP guidelines
- Highlight any lab or research experience on your CV
- Practice explaining how you stay organised
- Prepare examples of teamwork from school or work
- Check the company website to show genuine interest
Written by AI to help you understand this advert in plain English. It can get things wrong — always check the original advert before you apply.
Job description
Clinical Conduct Associate (Medical Research) Belfast, Northern Ireland Every member of the Celerion team is involved in making something essential a distinctive contribution to the health and well-being of people around the world. Thats the sense of purpose shared by employees throughout Celerion. We are an early phase drug research company, operating in robust and growing markets. We have an exciting future and offer a strong development environment for our excellent employees. We are looking…
How to apply
Applications are handled entirely by the employer on the original advert. We do not collect CVs, supporting statements or application data.
Provenance
Source
Adzuna
First seen
24 October 2026
Last checked
25 October 2026
Salary, closing date and description are taken from the employer's advert. The original advert always takes precedence.
About the employer
private
This listing was structured from Adzuna. Vacancy details and the application process remain the responsibility of the original source.
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