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The Sr. Director of Biostatistics will lead statistical activities for clinical trials, manage the biometrics team, and ensure collaboration with cross-functional teams to support regulatory submissions and data analyses.

The Senior Director of Data Management leads data management strategy for clinical programs, overseeing CRO partnerships, data lifecycle management, and compliance with regulatory standards. They mentor staff and ensure high-quality clinical data for submissions.

The Associate Director, Supply Chain will develop clinical supply strategies, manage logistics activities, and ensure compliance for clinical trials while overseeing vendor relations and inventory management.

The Senior Manager, Regulatory Affairs (CMC and Devices) will lead regulatory submissions, author key documents, and ensure compliance for clinical trials.