Top Tech Jobs & Startup Jobs in Boston, MA

The Vice President, Compliance oversees the Corporate Compliance Program, ensuring regulatory adherence, managing clinical supplies, and fostering a culture of accountability.

The Senior Manager of Supply Planning oversees global supply network performance, ensuring uninterrupted product supply, optimizing inventory, and conducting risk management analyses. This role collaborates with various teams to enhance planning capabilities and streamline supply chain processes using SAP and data-driven metrics.

The Sr. Manager/AD, Statistical Programmer will lead statistical programming for clinical studies, manage CROs, and ensure successful data analysis for regulatory submissions. Responsibilities include overseeing dataset creation, collaborating with clinical teams, and mentoring programming staff.

The Regulatory Specialist prepares global regulatory submissions, compiles documentation, supports regulatory strategies, and monitors regulatory guidelines.

The Associate Director, Contracts will manage agreements related to clinical, research, manufacturing, and commercial functions while providing legal support and ensuring compliance with regulations.

The Director leads the BEAM-302 program, managing drug discovery and development activities, ensuring alignment across functions, and driving operational excellence.

The role involves providing statistical strategy and oversight for clinical trials, working with CROs, and supporting regulatory submissions.

The IT Business Analyst supports Quality and Regulatory Systems, implementing modules, defining requirements, troubleshooting, and leading continuous improvement efforts.

The Senior Manager of Regulatory Affairs will develop and implement global regulatory strategies for genetic medicines, manage submissions, and ensure timely milestones are met.

The role leads U.S. promotional regulatory strategy, managing labeling documents and ensuring compliance with FDA regulations for gene editing products.