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The Senior Director of Statistical Programming leads the statistical programming function, manages resources, ensures quality of analysis and regulatory submissions, and drives innovation and standardization.

The role involves developing and executing US market access strategies for oncology therapeutics, managing payer marketing and contracting, and ensuring patient access while collaborating with cross-functional teams.

Lead and execute clinical development strategy for targeted oncology therapies, manage clinical trial processes, and collaborate with various stakeholders for regulatory compliance and safety monitoring.

Lead and develop the project management function at Immunome, ensuring high-quality support across Research and Development. Oversee team management and establish scalable project standards.

The Principal Scientist will optimize purification processes for mAbs, coordinate with CDMO partners, and oversee compliance and documentation for regulatory submissions.

The Principal Scientist will lead upstream process development for antibody intermediates, manage bioreactor experiments, and collaborate with CDMO partners.

The Manager, Supply Chain Systems oversees Immunome's digital supply chain platforms, focusing on NetSuite ERP, data governance, and analytics to streamline processes and improve data visibility.

The Executive Director, Investor Relations will manage investor relations and corporate communications, ensuring effective communication with investors and analysts, drafting core materials, and coordinating multiple stakeholders.

The Senior Clinical Trial Associate supports clinical study execution, manages study documentation, and ensures compliance with ICH-GCP and internal SOPs while coordinating with study teams and vendors.

The Principal/Senior Clinical Scientist will oversee clinical trials, design protocols, collaborate with teams, and mentor junior members.