Site Name: UK - London - New Oxford Street, Poznan Pastelowa Posted Date: Feb 21 2025 Senior Product Manager - Regulatory Vault (Veeva RIM) Are you passionate about making impactful contributions to the world of medicines and vaccines? GlaxoSmithKline (GSK) invites you to join our dynamic R&D Digital and Tech Team as a Senior Product Manager - Regulatory Vault. In this pivotal role, you will drive the vision and roadmap for the evolution of GSK's Regulatory Vault (Veeva RIM), ensuring our regulatory processes are streamlined and efficient. Your Role: As the Senior Product Manager - Regulatory Vault, you will be at the forefront of partnering with business owners across R&D and beyond. You will shape and define the vision for the technology that supports regulatory submissions and global license maintenance. Your responsibilities will include crafting product roadmaps and collaborating with our Managed Service Provider to deliver agile solutions that align with our strategic goals. Expertise in regulatory processes and systems and particularly like Veeva RIM is crucial, along with a proven ability to influence SaaS and Configurable Off-the-Shelf-products. About R&D Digital & Tech and Regulatory at GSK: At GSK R&D, we are driven by an ambitious goal to expedite submission cycle times and enhance submission quality across over 160 markets. Our investment in a cutting-edge Veeva RIM-based Regulatory Vault is a testament to our commitment to excellence. This platform is an integral part of a comprehensive Veeva ecosystem, supporting the entire development process. GSK stays dedicated to influencing Veeva's roadmap and extracting maximum value from our investments. Job Purpose: In this role, you will collaborate with GSK business process owners to design and implement features that simplify and enhance user experience, improve processes, and ensure compliance with global regulations. Working closely with Product leaders within Veeva and business stakeholders, you will map out processes and user journeys to prioritize and configure features in Veeva RIM. As a trusted advisor, you will remove blockers, foster collaboration, and consistently meet customer needs, delivering substantial value to GSK. Key Responsibilities: Develop a compelling roadmap and value propositions for future features that integrate processes across Development and beyond. Oversee the delivery, testing, and implementation of features in collaboration with our Managed Service Provider. Build a deep understanding of the GSK R&D Medicines and Vaccines Development process domain and contribute to strategy development. Lead teams, including strategic partners, to deliver features in compliance with internal security, risk management policies, and external regulatory requirements. Support formal testing and change management activities to prepare the business for the release of new features. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Bachelor's Degree or comparable experience in computer science or a related technical discipline. In-depth knowledge of Regulatory processes and systems, particularly Veeva RIM. Great experience delivering business impact through IT-enabled solutions in a life sciences context, with a background in business analysis and product ownership. Experience in Product Ownership within a major global IT organization, with a desire to enhance Product Leadership skills. Preferred Qualifications: If you have the following characteristics, it would be a plus: Veeva white belt certification. Experience with other Regulatory Processes and Platforms such as submission publishing (eCTD, non-eCTD) and Regulatory Intelligence. Excellent facilitation, communication, and interpersonal skills, with the ability to influence senior leadership using data and market evidence. A relentless focus on delivering business value and simplification, with a passion for advancing science and medicines. Experience managing solution delivery in a GxP context, with the ability to partner with Risk Management, Audit, and QA functions to ensure high-quality, compliant solutions. Strategic thinking, execution capabilities, and the ability to influence software partners and challenge business partners. Interested in Joining the Team? Join us at GSK and be a part of a team dedicated to making a difference in the lives of patients worldwide. Apply now to embark on a rewarding journey that combines collaboration, innovation, and impactful technology delivery. (Please take a personal copy of the Job Description, as this will not be available online post closure of the advert) Closing Date: 7th March 2025 DT Hybrid We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work. Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. 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