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Knowledge of clinical reporting requirements for medical devices, including GcP (Good Clinical Practice), MDSAP and European regulations governing medical devices. Works with the Technical Director and QARA Director on the handling of case report forms in accordance with regulatory requirements f...

Clinical Research Associate Position Description The Clinical Research Associate is responsible for ... medical and scientific journals or presented at meetings or conferences. 7. To operate within ...

... defence, and medical industry sectors. * Working closely with R&D teams to ensure the smooth integration of new products into the manufacturing process. * Work closely with production and ...

We work in partnerships with UK government customers and commercial providers to deliver research ... Private Health Scheme with no medical history checks, excess, or treatment limits * EV Salary ...

We work in partnership with UK government customers and commercial providers to deliver research ... Private Health Scheme, that disregards medical history, has no excess and no limit on treatments