Onsite Clinical Research Site Monitor

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.

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