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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 Milton Keynes, but within reach.
The Associate Director, Process Optimization & Digital Operations supports Clinical Risk Management by coordinating process optimization, digital landscape administration, and user support. They also manage super-user forums, vendor coordination, audit readiness, and governance logistics, ensuring consistent operation and user engagement across CRM tools and services.
The Associate Director, Digital Change Lead, is responsible for shaping the digital and data strategy for clinical risk management at Johnson & Johnson. This role involves leading the modernization of digital solutions, ensuring data quality and governance, and aligning with cross-functional teams to drive innovation and compliance.
The Manager, Quality Clinical Risk Management role involves leading and participating in clinical trial risk management activities, including risk identification, mitigation, and escalation. The role also supports pre-submission quality reviews, inspection readiness, and provides guidance on quality and compliance issues.
The role involves managing and overseeing clinical data sharing requests, ensuring compliance with privacy standards and procedural requirements. Responsibilities include supervising data anonymization vendors, managing YODA Project requests, and supporting external research teams using J&J clinical data.
This role involves leading the strategy, negotiation, and execution of global and local Pharmacovigilance Agreements, ensuring alignment with regulatory requirements and business objectives. The Director will manage a team responsible for alliance contracting, governance, compliance, and operational excellence, while fostering strong partnerships and driving continuous improvement and digital transformation.
This 12-month placement role involves hands-on experience in clinical and statistical programming, working with data integration, automation, and clinical insights. You will collaborate with experts to design and develop statistical solutions using tools like SAS, R, Python, and AI-driven technologies, contributing to the advancement of medical research and operational efficiency.
This role involves leading the development and maintenance of product labeling documents, providing guidance on labeling content and processes, and contributing to the global labeling strategy. The position requires a strong understanding of regulatory affairs and pharmaceutical drug development, with a focus on ensuring high-quality and compliant labeling.
This role involves servicing and maintaining a range of electro-mechanical equipment in medical and scientific environments across the Oxford, Banbury, Aylesbury, and surrounding areas. Responsibilities include fault-finding, equipment maintenance, and providing customer service. Full product training is provided.
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