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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
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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 outcomes
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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 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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Investigators, Trial Assistants and Assistant Trial Managers in applying for regulatory approvals for trials including MHRA, ethics, HRA and Research & Development (R&D) approvals. You will also be responsible
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, 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