Associate Director, Clinical Quality Lead; Fully Remote

• 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 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.

The Associate Director, Clinical Quality Lead (Fully Remote) position in the Legal, Management & Operations field is open for applications.