My client is a privately held, clinical stage, pre-IPO biotechnology company pioneering the development of vaccines through its investigational proprietary technology platform. The company has built a pipeline of four wholly-owned oncology programs, the lead of which is in Phase 2.

To support the growing clinical portfolio, my client is seeking a VP, Global Regulatory Affairs to play a key role in progressing innovative projects through pre-clinical and clinical development. This person will be responsible for providing global strategic and operational leadership for all drug development programs throughout all stages of clinical and commercial development.

• Developing successful global and country specific registration strategy for all development programs throughout all stages of clinical and commercial development
• Oversee and responsible for the preparation of all regulatory agency documents such as INDs, BLAs, Annual Reports
• Present a positive “hands on” attitude, a sense of urgency to get things done and demonstrate grace under pressure

Contact Heather Mudrick  heather@workforcegenetics.com