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

The Director of Field Force Operations will lead sales operations projects, enhance analytics, ensure data integrity, and drive commercial initiatives for effective growth in the pharmaceutical industry.

The Senior Director of CMC Process Development leads biologics process development, overseeing strategy, technical programs, external partnerships, and regulatory support. Must have expertise in biologics and management experience.

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.

The Head of Biomarker Development will set the biomarker strategy, oversee assay development, and contribute to regulatory submissions for neuromuscular and rare diseases.

The Head of Global GxP Quality will lead the Quality organization for both commercial and clinical operations, ensuring compliance and operational excellence. Responsible for strategy development, oversight of GMP, GCP, GLP, and Quality Systems, this role requires strong leadership to build a high-performing global team and represent quality during regulatory inspections.

The Director of Development Operations will support the CMO in managing development activities, facilitating communication, and improving operational efficiency within the organization.

The Director, National Accounts will lead strategic engagement with key payer accounts to ensure access to Scholar Rock's drug apitegromab, significantly impacting patient access and company launch success.