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About the Role:
- Responsible for GCP quality oversight of clinical development activities.
- Foundational role shaping GCP quality practices across the company.
What You Will Do:
- Lead GCP quality and manage deviations, investigations, and CAPA.
- Qualify, audit, and oversee CROs, sites, and clinical vendors.
- Partner with Regulatory Affairs and Technical Operations on health authority interactions and inspection readiness.
What You Bring:
- 10+ years of pharma/biotech experience including 8+ years hands-on GCP.
- Proven track record building GCP quality systems and leading sponsor audits.
- Independent, collaborative leader with strong communication skills.
Osanni Bio
Osanni Bio is a development-stage therapeutics platform headquartered in San Francisco, California, advancing programs in ophthalmology, cardiology, and beyond. They are a creative, agile team of innovators guided by core values of integrity, impact, agility, and collaboration.