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Manage the end-to-end clinical supply chain for multiple clinical programs, ensuring timely delivery of products while collaborating with various cross-functional teams and maintaining regulatory compliance.

The Associate Director will drive clinical strategy execution through collaboration, data analysis, project management, and coordination within teams to optimize processes and support clinical initiatives.

Lead statistical programming for clinical trials, managing programmers and CROs. Oversee programming activities, ensuring timely support for clinical projects and developing programming processes.

The Associate Director leads QC analytical testing, ensuring compliance with regulations, managing method validations, and collaborating on regulatory submissions.

The Senior Financial Analyst will enhance FP&A capabilities, support budgeting cycles, perform financial analysis, and collaborate across teams for reporting and forecasting.

The Associate Director oversees CRAs managing CRO monitoring for clinical trials, ensuring compliance, performance, and process development while leading teams and managing training.

Lead the biostatistics efforts for clinical studies, providing technical guidance, statistical analysis, and overseeing CRO teams while ensuring regulatory compliance.

Lead design, planning, execution, and quality oversight of clinical trial data management (Phase I-IV). Manage CROs and vendors, ensure EDC/eCRF/ CDM standards, support database locks/snapshots, collaborate with Biostatistics/Programming and other functions, and maintain regulatory-ready documentation for submissions.