IQVIA is seeking an on-site Clinical Monitoring professional in Langley, United Kingdom, to perform site monitoring visits (selection, initiation, monitoring and close-out) in accordance with GCP, ICH guidelines, and the contracted scope of work.
You will drive subject recruitment plans, administer protocol training to sites, manage regulatory submissions and TMF/ISF documentation, and collaborate with the study team to address issues and timelines.
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Berkshire
In this role you will lead monitoring and site management to ensure studies are conducted per protocol and regulatory requirements.
Reading
In this role you will lead monitoring and site management to ensure studies are conducted per protocol and regulatory requirements.
Reading
In this role you will monitor and manage clinical sites to ensure studies are conducted in line with the protocol, GCP, ICH guidelines, and sponsor…
Livingston
In this role you will monitor and manage clinical sites to ensure studies are conducted in line with the protocol, GCP, ICH guidelines, and sponsor…
Berkshire
In this role you will monitor and manage clinical sites to ensure studies are conducted in line with the protocol, GCP, ICH guidelines, and sponsor…
Manchester
In this role you will monitor and manage clinical sites to ensure studies are conducted in line with the protocol, GCP, ICH guidelines, and sponsor…
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