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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Onsite Clinical Research Site Monitor employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
