Manager, PVRM

Manager, PVRM at Sumitomo Pharma in Boise, Idaho, United States Job Description Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Safety Scientist Manager is responsible for providing pharmacovigilance and risk management support for assigned products across their lifecycle. This role works collaboratively with Pharmacovigilance (PV), Medical Safety, and cross-functional stakeholders to manage the benefit-risk profile of products, ensure patient safety, and support regulatory compliance. The position contributes to signal detection, aggregate safety reporting, safety governance forums, and inspection readiness activities, while serving as a subject matter expert within the assigned program(s). Job Duties & Responsibilities Benefit-Risk & Safety Surveillance + Work collaboratively with PV and cross-functional team members to manage the benefit-risk profile of assigned products and ensure patient safety. + Assist in signal detection activities, including data assembly, signal validation, and signal evaluation. + Perform literature monitoring (with vendor support) and ensure appropriate sources are incorporated into signal detection and ongoing safety surveillance activities. Aggregate Safety Reporting + Participate in and lead aggregate safety report activities, including data compilation, analysis, and writing of assigned sections, with vendor support as applicable. + Ensure high-quality, accurate, and inspection-ready contributions to periodic and ad hoc safety reports. Safety Governance & Cross-Functional Engagement + Compile agendas, data, presentation materials, and meeting minutes in collaboration with the Program Safety Lead for cross-functional Safety Management Team (SMT) meetings. + Represent PV Operations on cross-functional program and project teams and support PV Medical Safety activities as required. Ad Hoc Safety Issues & Regulatory Interactions + Coordinate responses to ad hoc safety issues and inquiries from regulatory authorities, clinical sites, or healthcare pro

Job Posting:

JC291595857

Posted On:

May 09, 2026

Updated On:

May 09, 2026