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coordination, administration, monitoring and data management. The successful candidate will have significant experience in the coordination of MHRA regulated clinical trials involving Investigational Medicinal
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, particularly in MHRA regulated trials involving Investigational Medicinal Products or Devices. About the Centre and Institute The Centre for Cardiovascular Medicine and Devices has been created to bridge the gap
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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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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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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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) guidelines, current MHRA Orange Guide including EU GMP regulations for ATMP manufacturing for clinical trials Awareness or knowledge in compiling Site Validation Master Plan covering aspects of site/equipment