Oruka Therapeutics

Provide strategic and operational leadership for clinical monitoring activities across Phase 1–3 trials, ensuring high-quality execution and CRO performance. Develop scalable clinical operations infrastructure, monitoring processes, and vendor oversight strategies within a biotech environment.

The MSL will develop and manage peer-to-peer relationships with healthcare professionals and key opinion leaders to support medical affairs objectives. They are responsible for executing territory engagement plans and providing internal stakeholders with actionable insights from the clinical community.

The MSL will develop and manage peer-to-peer relationships with healthcare professionals and key opinion leaders to support medical affairs objectives. They are responsible for executing territory engagement plans and providing internal stakeholders with actionable insights from the clinical community.

The MSL will develop and manage peer-to-peer relationships with healthcare professionals and key opinion leaders to support medical affairs objectives. They are responsible for executing territory engagement plans and providing internal stakeholders with actionable insights from the clinical community.

The Director of Clinical Quality Assurance provides strategic leadership and oversight for clinical development activities, ensuring compliance with GCP and global regulatory requirements. This role manages vendor quality, leads inspection readiness efforts, and supports continuous improvement across clinical quality systems.