The Senior Director, CMC Program Lead will oversee CMC development and manufacturing, coordinating across multiple functions to meet program milestones.

The Director of Quality Systems and GxP Compliance ensures compliance with regulatory standards, manages the quality management system, and leads the compliance team.

The Vice President, Head of Preclinical Sciences will lead preclinical development strategy and execution in toxicology, DMPK, and bioanalytical sciences to support IND submissions and clinical development of biologics.

The Vice President, CMC Technical Development will lead Scholar Rock's CMC development, overseeing drug substance, product formulation, and analytical development, while guiding global regulatory submissions and building a high-performing team.

The Director of FP&A R&D will oversee financial planning for R&D programs, supporting budgeting, forecasts, and strategic initiatives while ensuring effective communication across teams.