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Lead the development of total rewards strategy, oversee compensation plans, benefits administration, and recognition programs to enhance employee engagement.

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.

The Pharmacovigilance Operations Manager oversees global safety operations, vendor management, compliance, and cross-functional collaboration in clinical-stage oncology programs.

The role oversees CDMO operations, ensuring supply requirements, managing relationships, supporting contract negotiations, and monitoring performance to meet Immunome's biopharmaceutical needs.

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 Senior EDC Programmer leads the design and maintenance of clinical trial databases, ensuring compliance and quality data collection. They collaborate with multiple teams, oversee programming tasks, and contribute to documentation and SOP development.

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 analytical method development, validation, and QC activities for small molecules. Collaborate with cross-functional teams and manage external partners to support drug development and regulatory submissions.

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