Onsite Clinical Research Site Monitor
Listed on 2026-10-16
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Science
Clinical Research
IQVIA LLC is seeking an on-site Monitor/CRA to perform initiation, ongoing monitoring and close-out visits within interventional studies in the United Kingdom. You will drive subject recruitment plans, administer protocol training, maintain TMF/ISF, and escalate any quality findings.
The role requires a minimum of 2 years’ on-site monitoring experience, a degree in a scientific discipline or healthcare, and full UK right to work. Strong regulatory knowledge and communication skills are essential.
Our team is growing, and we are hiring a Onsite Clinical Research Site Monitor in Henley-on-Thames, England, United Kingdom.
This position is for the Onsite Clinical Research Site Monitor role at IQVIA LLC.
We are seeking a motivated Onsite Clinical Research Site Monitor to join IQVIA LLC in Henley-on-Thames, England, United Kingdom.
Consider building your career as a Onsite Clinical Research Site Monitor at IQVIA LLC.
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