Jobs at Oruka Therapeutics

The Associate Director, CMC Lead will provide strategic leadership for CMC activities in biologics, oversee technical operations, collaborate with internal teams and CDMOs, and ensure successful regulatory submissions.

This role involves leading device development for prefilled syringes and auto-injectors, integrating medical engineering and human-centered design, and ensuring compliance with regulatory standards throughout the product lifecycle.

The role oversees QA for clinical supply chain activities including compliance, oversight of IRT systems, labeling, distribution, and cold chain management supporting Phase 2 and Phase 3 programs.

The Administrative Assistant supports multiple teams, managing calendars, travel, expense reports, meeting logistics, and office inventory.

The Senior Publications Manager will lead publication planning and execution for clinical programs, collaborating with cross-functional teams and managing vendor relationships to ensure high-quality scientific communications.

The Director of Biostatistics will lead statistical strategy for clinical development programs, design studies, and provide statistical input for regulatory submissions while collaborating across teams.