-
Healthcare products Regulatory Agency (MHRA) and/or the Health Research Authority (HRA). The role holder will have experience in providing advice, guidance and training on all matters relating to research
-
, and other regulations applicable to clinical research governance as set by the Medicines and Healthcare products Regulatory Agency (MHRA) and/or the Health Research Authority (HRA). The role holder will
-
diverse and extends across several functions including sponsorship review for submissions to external bodies (including the Medicines and Healthcare products Regulatory Agency (MHRA)) and NHS research
-
regulatory bodies such as the Medicines and Healthcare products Regulatory Agency (MHRA), as well as advising researchers, you may also be involved in supporting clinical trial planning, and undertaking GCP
-
to NHS Research Ethics Committees and regulatory bodies such as the Medicines and Healthcare products Regulatory Agency (MHRA), as well as advising researchers, you may also be involved in supporting
-
, with the remainder of time worked either remotely or in the office. Some roles will need to be on site more regularly. Who are we? The Medicines and Healthcare products Regulatory Agency enhance and
-
with the safety guidelines issued by the Medicines and Healthcare products Regulatory Agency (MHRA), the potential bio-effects of MRI at different field strengths, and with safety procedures (quench
-
at all times. To be familiar with the safety guidelines issued by the Medicines and Healthcare products Regulatory Agency (MHRA), the potential bio-effects of MRI at different field strengths, and with