Director, Clinical Development Systems

Company Overview Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets. Position Overview The Director, Clinical Development Systems (CDS) provides strategic and operational leadership of Immunome’s clinical systems, responsible for advancing the Development function’s systems strategy, roadmap, and implementation plans, including Trial Master File (TMF), Clinical Trial Management System (CTMS), reporting, AI-enabled dashboards, and KPI analytics. The Director partners with Development teams, IT, Quality, Procurement, Finance, and external vendors to establish connected, inspection-ready, and business-aligned clinical systems capabilities to enable end-to-end visibility across studies, countries, sites, milestones, documents, issues, risks, clinical monitoring activities, enrollment, cycle times, and trial performance indicators. The Director will also lead a high-performing CDS team to partner with Study Teams on trial delivery, oversee day-to-day vendor management, and establish clinical systems best practices. Responsibilities Clinical Development Serve as a clinical systems leader for the Development function, providing operational input on technology strategy, enterprise platforms, delivery options, and vendor solutions. Develop and maintain the multi-year systems roadmap, aligning systems investments to business priorities, regulatory compliance, patient impact, and measurable value. Recommend and establish governance forums for clinical systems programs, contributing to prioritization, scope and risk management, adoption, and sustainment. Champion AI-enabled dashboards and advanced analytics that provide actionable insights into portfolio health, site performance, monitoring quality, TMF health, issue resolution, and operational risk, etc. Manage business cases, budgets, vendor delivery, strategic sourcing inputs, and value realization for the CDS portfolio. Clinical Systems Delivery Lead cross-functional planning and delivery of TMF and CTMS implementation and modernization, including business process design, configuration, data migration, integration validation, training, adoption, and change management . Deliver a connected clinical operations ecosystem improving visibility across studies and spanning study start-up, enrollment, monitoring, milestones, protocol deviations, TMF health, inspection readiness , to closeout. Partner with data and analytics leaders to define trusted KPIs, data sources, quality standards, access controls, reporting needs, and scalable dashboards for executive, functional, study, and operational teams. Identify and sponsor opportunities to simplify manual tracking, reduce duplicate data entry, automate processes, and strengthen data integrity. Vendor Management Lead vendor and platform selection, including RFPs, systems evaluations, and business case development. Oversee day-to-day management of vendors, ensuring vendor compliance with contractual obligations, timelines, and performance metrics. Quality and Regulatory Compliance Ensure adherence to ICH-GCP, FDA, EMA, and global regulatory requirements. Partner with Quality Assurance on system validation, inspection-readiness, audits and regulatory inspections, and corrective actions. Drive operational excellence to ensure data integrity . Budget and Resource Management…