The Head of Technical Operations leads CMC activities for clinical products, develops supply chain strategies, and presents to the Executive Team. Responsibilities include team leadership, external partnership management, and ensuring timely product supply for clinical operations.

The Director will lead medical writing efforts, ensuring high-quality clinical and regulatory documents while managing an internal team and collaborating cross-functionally.

The Legal Specialist provides legal assistance for contract development, negotiation, and compliance in clinical research and risk management.

The Associate Director of Program Management will oversee cross-functional drug development programs, manage timelines and budgets, and ensure effective communication and risk management.