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The Director, Regulatory Systems and Operations leads regulatory infrastructure, manages RIM systems, and ensures compliance while overseeing global regulatory deliverables.

The Senior Director, Regulatory Affairs CMC leads global CMC regulatory strategies, ensuring compliance with regulatory requirements and overseeing high-quality submissions and inspections across the product lifecycle.

Oversee Product and Pipeline Communications for vopimetostat, managing communications related to data, regulatory milestones, and commercial launch while collaborating with various teams.

The Associate Director, Corporate Counsel supports corporate governance and public reporting obligations, provides strategic legal guidance, manages SEC filings, and collaborates with senior executives and internal teams.

The Director of Compliance will lead compliance initiatives, develop policies, and provide training, ensuring adherence to healthcare regulations within a biotechnology company.

Lead clinical biomarker development and assay operations while collaborating across teams and managing vendor relationships for clinical trials.

The Site Management Leader oversees site management activities in clinical trials, ensuring compliance, managing risks, supporting site initiation, and monitoring patient recruitment.

The Central Operations Head oversees clinical drug supply and trial management, ensuring compliance, performance metrics alignment, and fostering a high-performing team for clinical development programs.

The Director of Biostatistics will lead statistical activities across clinical programs, optimize trial designs, collaborate with teams, and oversee statistical deliverables for regulatory submissions.

The Clinical Trials Manager will lead and manage the operational aspects of clinical trials, ensuring compliance with regulations and timelines, while coordinating with external partners and supporting team communication.