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The Senior Project Manager will oversee CMC processes in pharmaceutical development, coordinating cross-functional teams and managing timelines and budgets while ensuring alignment with organizational goals.

The Associate Director is responsible for managing early-stage programs, driving cross-functional planning, and ensuring timely execution through effective risk management and stakeholder engagement.

The Associate Director/Principal Scientist will lead clinical biomarker activities, oversee assay development, data analysis, and support oncological drug development at Immunome.

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

Define and implement the enterprise data architecture, manage data strategies, and collaborate with stakeholders to enable analytics and reporting for commercial readiness.

The Associate Director, Contracts Attorney will draft, negotiate, and manage various agreements while providing legal advice and ensuring compliance with legal standards.

The Principal Scientist leads pathology expertise to inform target biology and translational activities in oncology, evaluating tissues and collaborating across teams.

Lead integration of anatomic pathology in drug development, conduct tissue evaluation, guide advanced analysis, and ensure regulatory compliance.

The Contracts Attorney will draft, review, and negotiate contracts, manage the contract lifecycle, ensure compliance, and provide legal guidance on related matters.

Immunome is seeking proactive candidates to join their talent community for future job opportunities in oncology therapeutics. Interested applicants are encouraged to submit their resumes for consideration when relevant roles become available.