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As the Project Leader you will be responsible for acting as the Study Director / Principle Investigator / Responsible Scientist for assigned regulatory studies, and acting as the key contact for clients.
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Support project teams through (e)TMF and study document management, vendor management, assist with regulatory and ethics submissions. This TMF Expert will work closely with Clinical Project Managers across Phase I-III trials, covering multiple responsibilities of outsourced operational activities.
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As regulatory demands from the PRA and FCA continue to grow, there has never been a more crucial time for financial institutions to ensure the accuracy and compliance of their regulatory reporting, hence this crucial hire to join their dynamic London team.
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We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
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Supporting the Financial accountant with coordinating other local compliance obligations for all En Route entities and related intercompany journals and transfer pricing. Production of consolidated management accounts packs for submission to head office (multi-company & multi-currency.
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Conduct company investment research to an validate investment thesis – including financial analysis, due diligence on industry trends, company management and strategies and ESG impact and risks.
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As a Conflicts Analyst (remote) you will be responsible for identifying and managing potential conflicts of interest, ensuring compliance with regulatory requirements and company policies.
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With a specific focus on regulatory compliance and data quality, data science and innovative development of systems and tools, the RDO Analytics and Reporting team is accountable for maximising the business value of our global Regulatory business data.
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You will need a strong understanding of AML legal frameworks and sanctions regimes (applicable to money transfer, payments and e-money firms) and be able to offer commercial and proactive solutions whilst protecting the business, confidently articulating complex regulatory requirements to all stakeholders.
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Develop and implement a comprehensive QA strategy across operations, focusing on compliance with regulatory requirements, particularly in PEPs and Sanctions screening, Transaction Monitoring, KYC/KYB, Customer Services, and Complaints management.
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Yourgene also has a global laboratory service network equipped to be a full life-cycle partner for clinical, research and pharmaceutical organisations to support partners at the preclinical, clinical, and post market stage to develop, manufacture, obtain regulatory approval and commercialise new products and services.
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Experience negotiating ISDA and other OTC derivatives and advising on related regulatory issues pertaining to OTC derivatives. · Work with external advisors as required to define the regulatory requirements for crypto derivatives in various jurisdictions.
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This is a broad role with a particular focus on the following attributes - central compliance (i.e. preparation of management information, managing policies and procedures, keeping compliance logs, and regulatory reporting) and performing reviews as part of the compliance monitoring programme and KYC/AML controls.
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In House Counsel – VP – Regulatory Lawyer – Asset Management Sector – 4-6pqe - London. They are looking for a VP level Regulatory Lawyer with transactional experience to be in house advising their global markets team dealing with issues that arise from the trading and market facing activity of their funds and clients.
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We are looking for an Automotive Battery Research Engineer to join our client’s electric vehicle research team. For more information on the Automotive Battery Research Engineer role, please apply now.
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clinical research regulatory compliance project management jobs in United Kingdom
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