Senior Analyst, R&D Master Data

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: R&D Operations Job Sub Function: Clinical Supply Operations Job Category: Professional All Job Posting Locations: Beerse, Antwerp, Belgium Job Description: Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine We are searching for the best talent for Senior Analyst, R&D Central Master Data Purpose: The Senior Analyst, R&D Central Master Data, is responsible for the creation, maintenance, governance, and quality oversight of clinical finished goods master data in SAP S/4HANA and associated clinical supply planning systems. This role partners closely with Clinical Supply Chain, Trial Supply Leads, End-to-End Supply Planners, Supply Network Planners, Clinical Operations, Quality and other stakeholders to ensure master data accurately supports clinical trial planning, manufacturing, packaging, distribution, and forecasting activities. The individual will act as a subject matter expert for clinical supply master data processes, provide technical support for related systems, drive data quality and compliance, develop reporting and analytics, and contribute to continuous process improvement initiatives.   You will be responsible for: Lead the creation, maintenance, validation, and governance of clinical finished goods master data in SAP S/4HANA and related planning systems. Ensure master data accuracy, completeness, consistency, and compliance with established business processes, data standards, and regulatory requirements. Define, maintain, and continuously improve master data governance processes, procedures, standards, and controls. Serve as the functional Subject Matter Expert (SME) and Super User for SAP S/4HANA master data supporting clinical supply operations. Provide technical guidance, troubleshooting support, and issue resolution related to SAP S/4HANA master data and supply planning processes. Support the development, testing, and implementation of new master data requirements, system enhancements, and process improvements. Partner with business and IT teams to evaluate, design, and implement system changes impacting master data processes. Collaborate with cross-functional stakeholders to understand clinical trial requirements and translate business needs into scalable master data and system solutions. Maintain a deep understanding of clinical supply chain processes, trial design considerations, and planning system functionality to provide effective recommendations and support. Support user access management and system administration activities within clinical supply planning systems. Monitor data quality metrics, process compliance, and milestone completion, and communicate status, risks, and recommendations to business stakeholders. Develop, maintain, and deliver reports, dashboards, and analytics to support operational and strategic