Jobs at pliant-therapeutic

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.

Designs and executes in vitro and in vivo experiments for tissue-specific drug delivery, manages CRO studies, supervises research associates, analyzes and documents data, and communicates results to interdisciplinary teams to advance drug discovery programs.

Perform and optimize molecular and cell-based assays on cell and tissue samples, including immune cell isolation, flow cytometry, transfection, ELISA, and immunofluorescence. Maintain accurate records, analyze and report results, troubleshoot experiments, support research projects, and contribute to adoption of new technologies within the translational sciences team.

The Senior Director, Clinical Operations oversees and manages clinical studies, ensuring timely execution, GCP compliance, and development of budgets while leading the Clinical Operations team.