Teams at Pliant Therapeutics

Leads global Regulatory Affairs and Quality for oncology programs, including regulatory strategy, IND/CTA submissions, FDA and international health-authority interactions, GxP quality systems, audits, inspections, vendor oversight, and quality agreements. Advises executives on oncology pathways, supports pharmacovigilance and safety governance, evaluates partnerships, and scales the Regulatory and Quality organization, infrastructure, budget, and team.

The Senior Director, Clinical Operations will oversee clinical studies, ensuring compliance with GCP/ICH guidelines, managing budgets, and leading teams to achieve clinical trial goals.