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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