Clinical Reseach Associate - UK - multi-sponsor
Syneos Health
UKView on map(opens Google Maps in a new tab)
Salary
See original advert
Contract
Not specified
Hours
Full time
Closing date
Not specified
In plain English
What this job actually involves
You will support clinical trials by checking data and helping study sites. It suits people who like detail, organisation and working with others.
What you'll need
- A degree or similar qualification in a science subject
- Good organisational and time‑management skills
- Ability to follow strict study guidelines
- Basic computer and data entry skills
- Willingness to travel to trial sites as needed
How to boost your chances
- Add any lab, research or internship experience to your CV
- Read up on Good Clinical Practice (GCP) basics
- Give clear examples of teamwork in past roles
- Be ready to discuss how you handle travel for work
- Practice writing short, accurate reports
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 Reseach Associate - UK - multi-sponsor Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand custo…
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
20 September 2026
Last checked
17 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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