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senior project manager delegated authority london markets

Sanderson

Senior Project Manager / Programme Manager - Delegated Authority - London Markets Insurance Sanderson have been exclusively engaged by a leading london markets insurance organisation to recruit a Senior Project Manager or 'Hands on' Programme Manager. This will be working on the Delegated Authority workstream of a wider Consumer Duty Programme. This person will be working with a Big 4 Consulting Partner, Internal SME's and a range of Senior Business Stakeholders. This role is 2 to 3 days on site per week in Central London.Experience:- Vastly experienced Senior Project & Programme Manager- A proven record working within the London Markets / Speciality Insurance sector (ideally recently)- Delegated Authority Experience is ESSENTIAL- Consumer Duty or wider regulatory change is a nice to have- Excellent stakeholder management with a collaborative approachIf candidates could kindly just apply to the link then we will be in touch with people progressed. Thank you in advance. Reasonable Adjustments: Respect and equality are core values to us. We are proud of the diverse and inclusive community we have built, and we welcome applications from people of all backgrounds and perspectives. Our success is driven by our people, united by the spirit of partnership to deliver the best resourcing solutions for our clients. If you need any help or adjustments during the recruitment process for any reason, please let us know when you apply or talk to the recruiters directly so we can support you.<img src="https://www.jobg8.com/Tracking.aspx?vAeLusD9WE2RXVLM8D%2fDyF%2bcsOkM4K38b" width="0" height="0" />

Senior Project Manager - Delegated Authority - London Markets

Healthcare Businesswomens Association

Job Description Summary (12 days per month on-site) Location: London (The Westworks), United Kingdom or Dublin, Ireland Internal Job Title: Global Program Regulatory Associate Director Job Description We are looking for an experienced and proactive Senior Global Program Regulatory Manager to join our Global Regulatory Affairs team. The role involves directing the development and submission of regulatory documents, providing strategic direction and negotiating with agencies to expedite approvals. It also ensures timely approval and compliance of new and marketed products, and serves as a regulatory liaison throughout the product lifecycle. Major Accountabilities <ul> <li>Lead the implementation of regulatory strategies and operational activities across major global regions.</li> <li>Provide strategic input into global regulatory plans, identifying risks and contributing to key planning documents.</li> <li>Align regional regulatory approaches with global objectives through collaboration with cross-functional and regional teams.</li> <li>Define and manage Health Authority (HA) interaction strategies, including preparation of briefing materials.</li> <li>Oversee the planning, coordination, and submission of regulatory dossiers (e.g., CTAs, INDs, Risk Management Plans).</li> <li>Serve as a liaison with local HAs (e.g., FDA, EMA) and lead or support negotiations for regional approvals.</li> <li>Develop and implement strategies to minimize review delays and regulatory clock stops.</li> <li>Ensure timely and compliant responses to HA queries and requests.</li> <li>Contribute to departmental goal setting and lead initiatives to improve regulatory processes.</li> <li>Ensure adherence to internal policies, SOPs, and global regulatory requirements.</li> </ul> Minimum Requirements <ul> <li>Bachelor's or Master's degree in Life Sciences, Pharmacy, or a related field.</li> <li>Significant experience in regulatory affairs within the pharmaceutical industry.</li> <li>Proven track record in project management and regulatory operations.</li> <li>Experience representing the organization in cross-functional and cross-cultural settings.</li> <li>Strong knowledge of clinical trials, drug development, and regulatory compliance.</li> <li>Excellent problem-solving, negotiation, and communication skills.</li> <li>Detail-oriented with the ability to manage complex regulatory projects.</li> <li>Skilled in risk management and working with cross-functional teams.</li> <li>Ability to navigate and influence Health Authority interactions.</li> <li>Fluency in English (written and spoken) is essential.</li> </ul> Commitment to Diversity and Inclusion/EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Skills Desired <ul> <li>Clinical Trials</li> <li>Cross-Functional Teams</li> <li>Detail-Oriented</li> <li>Drug Development</li> <li>Lifesciences</li> <li>Negotiation SkillsProblem Solving SkillsRegulatory ComplianceRisk Management</li> </ul><img src="https://www.jobg8.com/Tracking.aspx?vAeLusD9WE0pILu4uWEJNiiMBr948H6fb" width="0" height="0" />

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

Penguin Recruitment Ltd

Assistant Town Planner / Town Planner London Private Consultancy Flexible Working Excellent Career Progression Are you a motivated Assistant or Town Planner with 1-3 years of experience looking to take the next step in your planning career? I'm working with a leading independent planning consultancy in London, who are looking to add a talented Planner to their close-knit and growing team. The company has a strong reputation for delivering high-quality planning advice across residential, commercial, mixed-use and regeneration schemes throughout London and the South East. You'll work alongside experienced Directors and Senior Planners, gaining exposure to a wide variety of projects and the opportunity to develop both technically and professionally. The RoleAs an Assistant or Town Planner, you'll be involved in: <ul> <li>Preparing and submitting planning applications, appeals, and Local Plan representations</li><li>Conducting site appraisals and research</li><li>Supporting senior colleagues on complex projects and client meetings</li><li>Liaising with local authorities, clients, and consultants</li><li>Preparing reports and planning statements</li></ul> Requirements <ul> <li>1-3 years of experience in a planning role, ideally within a consultancy or local authority</li><li>RTPI accredited degree in Town Planning or related subject</li><li>Strong written and verbal communication skills</li><li>A proactive attitude and passion for planning in the private sector</li><li>Working towards or recently achieved RTPI Chartership</li></ul> Benefits <ul> <li>Competitive salary DOE</li><li>Generous annual leave and pension</li><li>Hybrid working (2-3 days in the office)</li><li>Ongoing support with RTPI Chartership</li><li>Excellent career development opportunities within a collaborative team</li></ul> This is an excellent opportunity to join a respected consultancy where you'll work on a diverse range of projects and be supported to progress your career quickly. To apply or find out more, contact Josh Jones at Penguin Recruitment on or email <img src="https://www.jobg8.com/Tracking.aspx?vX6ucqYYTOaR1U9L%2fjsHK0xV3GzWMd7Dv" width="0" height="0" />

Assistant Town Planner

Novartis Farmacéutica

Choose LocationChoose Location# Global Regulatory Affairs Associate Director (Cardio-Metabolic)REQ-Oct 14, 2025United Kingdom Summary (12 days per month on-site) Location: London (The Westworks), United Kingdom or Dublin, Ireland Internal Job Title: Global Program Regulatory Associate Director We are looking for an experienced and proactive Senior Global Program Regulatory Manager to join our Global Regulatory Affairs team.The role involves directing the development and submission of regulatory documents, providing strategic direction and negotiating with agencies to expedite approvals. It also ensures timely approval and compliance of new and marketed products, and serves as a regulatory liaison throughout the product lifecycle. About the Role Major accountabilities: Lead the implementation of regulatory strategies and operational activities across major global regions. Provide strategic input into global regulatory plans, identifying risks and contributing to key planning documents. Align regional regulatory approaches with global objectives through collaboration with cross-functional and regional teams. Define and manage Health Authority (HA) interaction strategies, including preparation of briefing materials. Oversee the planning, coordination, and submission of regulatory dossiers (e.g., CTAs, INDs, Risk Management Plans). Serve as a liaison with local HAs (e.g., FDA, EMA) and lead or support negotiations for regional approvals. Develop and implement strategies to minimize review delays and regulatory clock stops. Ensure timely and compliant responses to HA queries and requests. Contribute to departmental goal setting and lead initiatives to improve regulatory processes. Ensure adherence to internal policies, SOPs, and global regulatory requirements. Minimum requirements: Bachelor's or Master's degree in Life Sciences, Pharmacy, or a related field. Significant experience in regulatory affairs within the pharmaceutical industry. Proven track record in project management and regulatory operations. Experience representing the organization in cross-functional and cross-cultural settings. Strong knowledge of clinical trials, drug development, and regulatory compliance. Excellent problem-solving, negotiation, and communication skills. Detail-oriented with the ability to manage complex regulatory projects. Skilled in risk management and working with cross-functional teams. Ability to navigate and influence Health Authority interactions. Fluency in English (written and spoken) is essential. Commitment to Diversity and Inclusion/EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Why Novartis: Join our Novartis Network: Benefits and Rewards: Read our handbook to learn about all the ways we'll help you thrive personally and professionally:DevelopmentUniversal Hierarchy NodeUnited KingdomLondon (The Westworks)GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd.Research & DevelopmentFull timeRegularNoNovartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.REQ- Global Regulatory Affairs Associate Director (Cardio-Metabolic)<img src="https://www.jobg8.com/Tracking.aspx?n70Gs5vBCd8IWwUuLMXZlaNb9isvX8%2f5f" width="0" height="0" />

London Stock Exchange Group

About the Role We are seeking a highly experienced and strategically minded Programme Delivery Assurance Director to join our Group Investment Management Team . This pivotal role will lead delivery assurance activity comprising review and challenge of sophisticated technical transformation programmes, which in practice means identifying 'what's going wrong' and working out 'how to fix it' at the earliest opportunity. Additionally, you'll review programmes to ensure alignment with the Group Delivery Disciplines (GDDs) and focus on driving continuous improvement across the change portfolio.The Programme Delivery Assurance Director will input into the Group Investment Committee (GIC) , providing insights on delivery assurance findings, and remediation actions. This role requires a blend of strategic oversight, hands-on programme assurance, and customer engagement across internal and external partners. Key Responsibilities Lead and coordinate deep-dive delivery assurance reviews on complex and technial programmes using GDDs as the framework to review against. Identify early indicators of delivery risk and support root cause analysis and resolution planning Track and report on delivery assurance-related Capex recovery Provide regular updates to the GIC on delivery assurance findings, risks, and remediation progress Engage with Delivery Portfolios to monitor delivery assurance compliance. Collaborate with the Transformation Community to communicate delivery assurance expectations and share insights Build and maintain relationships with external delivery assurance specialists to support technical, design, and engineering reviews Identify programmes requiring enhanced delivery assurance through system-driven metrics and performance indicators Drive the evolution of Group Delivery Disciplines based on delivery assurance insights and lessons learned Promote best practices and knowledge sharing across the investment and transformation communities Required Experience & Qualifications Confirmed experience as a Programme Director or senior-level Programme Manager, with hands-on experience of delivering complex transformation programmes including large system implementations Validated experience in a senior delivery assurance role within a complex, multi-programme environment Proven experience of using the software development lifecycle (SDLC) and project management methodologies including agile, waterfall and hybrid project management (qualifications or equivalent certifications crucial) Strong understanding of capital investment governance, delivery frameworks, and risk management Ability to lead deep-dive reviews and influence senior customers Experience working with external delivery assurance providers and running third-party assurance engagements Familiarity with engineering and technical quality assurance practices, including delivery and testing metrics and root cause analysis Familiarity with Product Management principles Experience and Qualifications Required Strategic problem solver with strong analytical and problem-solving skills Excellent communication and stakeholder management abilities Ability to work across multiple programmes and adapt to changing priorities Deep understanding of delivery methodologies and assurance frameworks Collaborative leadership style with a focus on continuous improvementLSEG (London Stock Exchange Group) is a leading global financial markets infrastructure and data provider. Our purpose is driving financial stability, empowering economies and enabling customers to create sustainable growth. Our culture of connecting, creating opportunity and delivering excellence shapes how we think, how we do things and how we help our people fulfil their potential.Working with us means that you will be part of a dynamic organisation of 25,000 people across 65 countries. However, we will value your individuality and enable you to bring your true self to work so you can help enrich our diverse workforce. You will be part of a collaborative and creative culture where we encourage new ideas and are committed to sustainability across our global business. You will experience the critical role we have in helping to re-engineer the financial ecosystem to support and drive sustainable economic growth. Together, we are aiming to achieve this growth by accelerating the just transition to net zero, enabling growth of the green economy and creating inclusive economic opportunity.LSEG offers a range of tailored benefits and support, including healthcare, retirement planning, paid volunteering days and wellbeing initiatives.We are proud to be an equal opportunities employer. This means that we do not discriminate on the basis of anyone's race, religion, colour, national origin, gender, sexual orientation, gender identity, gender expression, age, marital status, veteran status, pregnancy or disability, or any other basis protected under applicable law. Conforming with applicable law, we can reasonably accommodate applicants' and employees' religious practices and beliefs, as well as mental health or physical disability needs.Join us and be part of a team that values innovation, quality, and continuous improvement. If you're ready to take your career to the next level and make a significant impact, we'd love to hear from you.LSEG is a leading global financial markets infrastructure and data provider. Our purpose is driving financial stability, empowering economies and enabling customers to create sustainable growth.Our purpose is the foundation on which our culture is built. Our values of Integrity, Partnership , Excellence and Change underpin our purpose and set the standard for everything we do, every day. They go to the heart of who we are and guide our decision making and everyday actions.Working with us means that you will be part of a dynamic organisation of 25,000 people across 65 countries. However, we will value your individuality and enable you to bring your true self to work so you can help enrich our diverse workforce.We are proud to be an equal opportunities employer. This means that we do not discriminate on the basis of anyone's race, religion, colour, national origin, gender, sexual orientation, gender identity, gender expression, age, marital status, veteran status, pregnancy or disability, or any other basis protected under applicable law. Conforming with applicable law, we can reasonably accommodate applicants' and employees' religious practices and beliefs, as well as mental health or physical disability needs.You will be part of a collaborative and creative culture where we encourage new ideas. We are committed to sustainability across our global business and we are proud to partner with our customers to help them meet their sustainability objectives. Our charity, the LSEG Foundation provides charitable grants to community groups that help people access economic opportunities and build a secure future with financial independence. Colleagues can get involved through fundraising and volunteering.LSEG offers a range of tailored benefits and support, including healthcare, retirement planning, paid volunteering days and wellbeing initiatives.Please take a moment to read this carefully, as it describes what personal information London Stock Exchange Group (LSEG) (we) may hold about you, what it's used for, and how it's obtained, .If you are submitting as a Recruitment Agency Partner, it is essential and your responsibility to ensure that candidates applying to LSEG are aware of this privacy notice.LSEG (London Stock Exchange Group) is a leading global financial markets infrastructure and data provider. Our purpose is driving financial stability, empowering economies and enabling customers to create sustainable growth. Our culture of connecting, creating opportunity and delivering excellence shapes how we think, how we do things<img src="https://www.jobg8.com/Tracking.aspx?BrmZWvLiuv7xDvcinGKSXzTLlB5nBaiHs" width="0" height="0" />

Technical Programme Manager, Delivery Assurance

ANRA Technologies, LLC

As a Technical Project Manager at ANRA Technologies, you will play a key role in driving strategic initiatives, coordinating cross-functional teams, and ensuring the successful delivery of cutting-edge solutions in the rapidly evolving drone industry.You'll bring strong project management expertise paired with an understanding of software engineering principles. You should thrive in an agile environment with minimal supervision and embrace continuous improvement and test-driven development.If you're a driven, collaborative leader who's ready to shape the future of drone technology, we'd like to meet you. Employment: Full Employment City Greater London, UK Schedule: Full Time / Hybrid Experience: 5+ years About ANRA ANRA Technologies, with offices in Washington DC, London, New Delhi and Estonia, is an international provider of drone operations and traffic management solutions for unmanned aircraft systems (UAS) aka Drone operators and airspace managers. We offer intelligent Machine Learning and AI driven traffic management software capabilities for UAS Traffic Management (UTM) and Urban Air Mobility (UAM) operations like "Flying Cars". Key Responsibilities <ul><li>Coordinate and lead an international, distributed team of software developers.</li><li>Ensure all projects are delivered on time, within scope, and within budget.</li><li>Define project scopes and objectives, engaging all relevant stakeholders and ensuring technical feasibility</li><li>Create and maintain comprehensive project documentation.</li><li>Collaborate to deliver robust, cloud-based solutions interoperable with global aviation standards.</li><li>Prepare and review technical proposals and documentation.</li><li>Stay abreast of emerging aviation technologies and industry trends; experiment and encourage innovation within the team.</li><li>Represent ANRA in technical discussions with customers, industry groups, standard development organizations, and government entities.</li><li>Travel occasionally for project support, customer meetings, and speaking engagements.</li></ul> Qualifications <ul><li>Bachelor's degree in Software Engineering, Computer Science, or a related technical field</li><li>5+ years of experience in end-to-end product delivery.</li><li>5+ years in technical project management, technical consulting, or engineering roles.</li><li>Proven experience managing technical projects using Agile methodologies; experience with Scrum frameworks is a plus.</li><li>Skilled in presenting and reviewing results with senior management and diverse stakeholders.</li><li>Strong interpersonal, verbal, and written communication skills.</li><li>Comfortable working in a fast-paced, collaborative, and innovative environment.</li><li>Proficient with Google Suite and project management tools.</li><li>PMP certification is a plus.</li><li>Aviation or drone industry experience is a plus.</li></ul><img src="https://www.jobg8.com/Tracking.aspx?jJgsV495VLeZUvzdhEXmRVCZ3WzlGXBOw" width="0" height="0" />

Technical Project Manager - UK

Groupe BPCE

This role involves the day-to-day management of Global Markets Operations (GMO) in the UK and EMEA oversight.As Head of GMO UK, you will manage and control the processing of all London-originated Global Markets transactions. Your responsibilities include delivering operational efficiency and ensuring appropriate controls for transactions booked and processed in London, as well as those booked in London but processed in Paris.You will supervise the processing of Global Markets transactions, monitor process performance in line with global standards, and own the booking processes, continuously seeking improvements, streamlining operations, and enhancing safety across functional silos, geographies, and business units.You will contribute to strategic initiatives for the CIB and COO, including projects like Front to Ops, and manage regulatory transaction reporting.Management of Global Market Operations (GMO) UK circa 70%)<ul><li>Organize and lead the UK team and coordinate with the EMEA GMO team, including projects and staff management.</li><li>Supervise transaction processing, monitor process performance, and act as an escalation point for GMO matters.</li><li>Ensure global consistency through the implementation of best practices and processing guidelines.</li><li>Coordinate projects between Head Office and local sites.</li><li>Monitor controls regionally to reduce operational risks.</li><li>Contribute to financial monitoring, including costs, headcounts, and budgets, collaborating with country COOs.</li><li>Set objectives and evaluate performance for GMO teams, participating in the ACR process with country COOs, specifically for UK.</li><li>Lead departmental restructuring and daily management, striving for operational excellence.</li><li>Implement good management practices, promote a performance culture, and develop strong relationships with London and Head Office operations.</li><li>Ensure high-quality service delivery to internal clients (Front Office, Sales, Traders) and external clients.</li><li>Support new business initiatives, develop solutions, and manage internal controls and reconciliations to reduce risks.</li><li>Maintain comprehensive knowledge of trade lifecycles and coordinate with teams in Paris and other control functions.</li><li>Analyze, report, and resolve issues, developing management dashboards and reports.</li></ul>Drive operational efficiency projects across UK and EMEA based on regional business lines.Skills required include strong knowledge of Global Market Products, operations experience in Commodities, Rates, Credit, FX, Equity, understanding of trade processes, regulatory requirements, GM systems architecture, process improvement, people management, change management, strategic thinking, and vendor management.<img src="https://www.jobg8.com/Tracking.aspx?3T4Xc8xAqRlkJiluYR%2b8WPm0gnkH64%2fYp" width="0" height="0" />

Head of Global Markets Operations UK

Explore 192+ Senior project manager delegated authority london markets in London United Kingdom this November. Find roles across top companies and apply now to boost your career.

192 senior project manager delegated authority london markets jobs IN London United Kingdom

Senior Project Manager - Delegated Authority - London Markets

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

Assistant Town Planner

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

Technical Programme Manager, Delivery Assurance

Technical Project Manager - UK

Head of Global Markets Operations UK