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This role involves leading the regulatory strategy for a cardiology medical device company, focusing on FDA, CE, and UKCA submissions, and ensuring compliance with international regulations. You will work closely with the senior team and regulatory bodies, driving the company's expansion into new markets.
The Data Sharing Manager is responsible for managing and overseeing the end-to-end process of internal and external data sharing requests, ensuring compliance with privacy standards and procedural requirements. The role involves supervising vendors, managing YODA Project requests, and providing support to external research teams using J&J clinical study data.
The Data Sharing Manager is responsible for managing and overseeing the end-to-end process of internal and external data sharing requests, ensuring compliance with privacy standards and procedural requirements. Key responsibilities include vendor oversight, YODA Project management, and supporting external research teams using J&J clinical study data.
The Manager Clinical Data Transparency, Data Sharing role involves managing and overseeing the end-to-end process of internal and external data sharing requests, ensuring compliance with privacy standards and procedural requirements. Responsibilities include supervising vendors for data anonymization, managing YODA Project requests, and supporting external research teams using J&J clinical study data.
The Senior Analyst role involves validating and adopting global PLAN business processes for the Transcend EMEA-OTC releases. Key responsibilities include driving process scoping, testing, and quality assurance, ensuring operational readiness, and facilitating continuous process improvements.
The Senior Analyst role involves validating and adopting global PLAN business processes for the Transcend EMEA-OTC releases. Key responsibilities include driving process scoping, testing, and quality assurance, ensuring operational readiness, and facilitating continuous process improvements.
A little outside Norwich, but within reach.
The QA Officer will work within an experienced team to maintain high quality standards in a GMP manufacturing environment. Responsibilities include controlling quality documentation, developing training programs, investigating GMP breaches, and supporting audits and continuous improvement projects.
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