PpWe are seeking an experienced Business Process Lead to support and lead Regulatory Information Management (RIM) transformation programmes within the Life Sciences industry. The role will focus on driving end-to-end regulatory business process design, process harmonisation, and implementation readiness as part of large-scale Veeva Vault RIM implementations. /p pThe successful candidate will combine strong regulatory domain expertise with consulting, stakeholder management, and delivery leadership capabilities to support global transformation programmes across Regulatory Affairs organisations. /p h3Key Responsibilities /h3 ul liLead regulatory business process workstreams within Veeva Vault RIM implementations /li liFacilitate and lead global workshops with business and IT stakeholders across Regulatory Affairs functions /li liDrive future-state process design, process mapping, gap assessments, and requirements definition /li liTranslate business requirements into user stories, functional requirements, acceptance criteria, and process documentation /li liSupport configuration discussions and alignment between business, architecture, integration, and development teams /li liSupport implementation planning, business readiness, change management, and adoption activities /li liWork closely with migration, testing, validation, and integration teams to ensure alignment across workstreams /li liSupport governance, RAID management, status reporting, and executive stakeholder communications /li liContribute to proposal development, solution shaping, effort estimation, and client presentations /li liSupport agile delivery methodologies including SAFe, Scrum, and sprint-based execution models /li /ul h3Required Skills Experience /h3 ul li8+ years of experience within Life Sciences, Regulatory Affairs, or Pharma RD transformation programmes /li liStrong experience supporting or leading Veeva Vault RIM implementations /li liDeep understanding of Regulatory business processes including: /li liSubmission Management /li liRegistration Management /li liHealth Authority Interactions /li liRegulatory Planning /li liProduct Application Lifecycle Management /li liExperience facilitating business process workshops and managing senior stakeholders globally /li liExperience writing user stories, requirements, process maps, and functional specifications /li liStrong understanding of regulatory data flows, integrations, and cross-functional dependencies /li liExperience working within agile delivery environments (SAFe, Scrum, Kanban) /li liExcellent communication, consulting, and stakeholder management skills /li liAbility to work across global teams, functions, and time zones /li liVeeva Vault RIM certification(s) /li liExperience with Regulatory data strategy, migration, testing, or validation activities /li liExperience with cloud-based RD platforms (e.g., Veeva Vault, CTMS, eTMF, Promomats) /li liConsulting experience within large-scale transformation programmes /li liUnderstanding of emerging regulatory requirements and compliance frameworks /li /ul pWe believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, sexual orientation, gender identity or expression, marital status, citizenship status or any other basis as protected by applicable law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities. /p /p #J-18808-Ljbffr