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Drafts, reviews, negotiates, and manages clinical and operational agreements, including clinical trial, confidentiality, master services, consulting, and informed consent agreements. Advises stakeholders on contractual risks, intellectual property, indemnification, liability, confidentiality, compliance, and regulatory considerations. Maintains templates, playbooks, and contract workflows; supports lifecycle management, audits, training, issue resolution, and process improvements across clinical operations.

Manage the company’s contract lifecycle, including intake, routing, drafting, review, execution, tracking, archiving, renewals, and risk assessment. Administer CLM systems, maintain templates and workflows, ensure compliance, and collaborate with R&D, Finance, Clinical, and other stakeholders. Support standard agreements such as NDAs, consulting agreements, SOWs, clinical trial agreements, MTAs, and vendor contracts.

Coordinates onsite and virtual interviews across multiple roles, serves as a primary candidate contact, organizes kickoff, debrief, and offer meetings, maintains accurate ATS records, and supports candidate travel, expenses, and onboarding logistics. Partners with recruiters and hiring teams to deliver an organized candidate experience in a fast-paced biotech environment.

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 Global Regulatory Lead will develop and execute regulatory strategies for therapeutic projects, ensuring compliance and success in submissions while leading cross-functional teams and managing risks.

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.