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Experience of collaborative interdisciplinary working Knowledge of information governance and compliance management including GDPR, REC, MHRA Committed to equality, diversity and inclusion, actively
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are submitted to MHRA, thereby maintaining Clinical Trial Authorisations To set up, initiate, monitor and close clinical trials on behalf of the sponsor where one or more of the partner institutions
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The MHRA is transforming. Through enabling innovation, making the right judgements of the benefits and risks of medical products and forging the right partnerships in the UK and internationally, it
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; The Medicines And Healthcare Products Regulatory Agency | Canary Wharf, England | United Kingdom | 30 days ago
The MHRA is transforming. Through enabling innovation, making the right judgements of the benefits and risks of medical products and forging the right partnerships in the UK and internationally, it
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and ensure on-going adherence to the requirements of the regulatory bodies i.e. NHS Health Research Authority, Research Ethics Committee (REC) and the Medicine Healthcare products Agency (MHRA); and
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Contract: Full Time/12 month fixed term contract The MHRA is transforming. Through enabling innovation, making the right judgements of the benefits and risks of medical products and forging
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the Medical Healthcare products Regulatory Agency (MHRA) and will link with the UK Clinical Research Collaboration (UKCRC) QA Subgroup. The successful candidate should have a first degree in a relevant subject
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& Social Care Research A sound knowledge of the principles of Good Clinical Practice Experience of making applications to regulatory bodies (MHRA) and to ethical committees via IRAS Experience of managing
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the regulatory guidelines of 'Good Manufacturing Practice' as defined in current version of the MHRA `Rules and Guidance for Pharmaceutical Manufacturers and Distributors', also known as the Orange Guide. You will
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stakeholders including doctors, patients, pharmacists, medical regulators and policy makers, such as MHRA, UKHSA. About you The successful applicant will be able to present information on research progress and