Regulatory affairs manager job in Bebington

... landscape, the ability to stay on top of new legislation and regulatory requirements, proactively manage legal affairs and manage our corporate and personal data effectively is crucial. We have a fantastic team of professionals who are passionate about what they do, ready to drive forward our strategy and support all of Capita in making a tangible impact. About Capita Capita is an outsourcer,

... patients as efficiently and effectively as possible.The Regulatory Affairs Director (RAD) provides strategic and operational regulatory leadership to the development, commercialization and life cycle management of assigned oncology products. Serves as the global regulatory lead (GRL) on early stage projects or specific indications of larger programs and/or as the regional regulatory lead. The

... Policy Analysis and Advocacy: Monitoring and analyse legislative, regulatory, and political developments relevant to Capita. Preparing briefings and summaries on policy issues impacting the organisation. Develop and execute advocacy strategies to influence public policy in alignment with organisational goals. Stakeholder Engagement: Building and maintaining relationships with government offici

... process.The Head (Senior Director) International CMC Regulatory Affairsreports to the Executive Director, International Regulatory Strategy and is accountable for and leading a team of regulatory professionals (7-10 direct reports at Director level and 30-40 indirect reports) responsible for strategy, delivery and execution of international CMC Regulatory strategy and leadership across the pro

... Job Description Summary . Job Description JOB TITLE: Head of Group Regulatory Policy– Corporate Affairs LOCATION(S): London Salary: £124,653 - £146,650 HOURS: Full time WORKING PATTERN: Hybrid, 40% (or two days) in our London Office About this opportunity We have an opportunity for a Senior Policy professional to join us in our Group Corporate Affairs team in London. Our team shapes

... Job Share Job Description Summary . Job Description JOB TITLE: Group Regulatory Policy Senior Manager – Corporate Affairs (Communications) LOCATION(S): London HOURS: Full time WORKING PATTERN: Hybrid, 40% (or two days) in our London office About this opportunity We're looking for an experienced Senior Policy professional to join our Group Corporate Affairs function to support our Group Re

... internal security, risk management policies and practices, external regulatory and statutory requirements Orchestrate our stage gate/demand process to bring ideas to new IT solutions, helping Development to identify and promote the most beneficial ideas Guide a product-oriented IT team that owns E2E all GRA IT solutions Act as program manager and ensure excellence in project set-up and executi

... for a Legal Counsel, Employment Litigation to join our Legal, Regulatory Affairs, Ethics & Compliance, and Secretariat Function (LRECS). LRECS focusses on providing a diverse and inclusive environment with a strong emphasis on wellbeing and delivering opportunities for growth and personal development. This is a new role created primarily to manage and run the Employment Tribunal claims ari

... Group functions operational activities. Monitoring Group functions regulatory compliance in relation to Operational Resilience and provide updates to senior management and to the PRA, as requested by the Compliance & Regulatory Affairs teams. Managing the governance of Operational Resilience for Group functions and report management information to the Operational Resilience Local Policy Sp

... activities related to late-stage trials leading to drug approval by regulatory agencies, including phase 2 and 3 clinical trials.As a Global Clinical Program Lead, you will work cross functionally to support the design, conduct, monitoring and data interpretation across a cluster of indication-aligned studies. GCPLs are strategic and patient focused, generating opportunity with an ambitious ap

... and interpretation, while influencing clinical development, regulatory, and commercial strategies. Collaborate with internal and external partners to meet business needs, including reviewing Investigator Sponsored Research (ISR) and GSK-sponsored Phase IV trials. Develop and apply novel statistical methodologies to address challenges in market access and reimbursement, partnering with global a

... strategic direction for HCP engagement Work hand in hand with global regulatory, global medical science, CGO marketing, global pharmacy sales and the countries to develop HCP strategies, HCP relevant evidence pipelines, evidence communication plans, NPD/EPD/BDI pipeline and copy approval of HCP toolkits Creation of compelling and HCP validated communication narratives which are brought to life

... Stakeholder Engagement, Project Management, Data Analysis, Regulatory Compliance, Cross-Functional Collaboration, Reporting and Communication, Environmental Management Systems, Auditing, Risk Management, Sustainable Sourcing, Training and Education, Life Cycle Assessment, Regulatory Knowledge, Human Rights, Due Diligence, International Standards, Stakeholder Collaboration, Training and Capacit