pliant-therapeutic Benefits Overview

Leads Pliant’s integrated Regulatory Affairs and Quality organization for early-phase oncology programs. Owns global regulatory strategy, IND/CTA submissions, FDA and international health-authority interactions, inspection readiness, and oncology regulatory designations. Oversees a risk-based GxP quality system spanning GLP, GCP, GVP, and GMP, including audits, vendor oversight, quality agreements, SOPs, and compliance metrics. Advises executives, supports safety and business-development activities, and scales team structure, systems, budget, and capabilities as the pipeline matures.