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This role involves leading device development for prefilled syringes and auto-injectors, integrating medical engineering and human-centered design, and ensuring compliance with regulatory standards throughout the product lifecycle.

The role oversees QA for clinical supply chain activities including compliance, oversight of IRT systems, labeling, distribution, and cold chain management supporting Phase 2 and Phase 3 programs.

The Accounting Manager oversees accrual processes for clinical trials, collaborates with teams for data analysis, prepares journal entries, and ensures compliance with accounting standards and internal controls.

The Senior Publications Manager will lead publication planning and execution for clinical programs, collaborating with cross-functional teams and managing vendor relationships to ensure high-quality scientific communications.

The Senior Paralegal/Senior Contracts Manager will manage the contracts lifecycle, support legal matters, and maintain corporate records for a biopharma company, ensuring compliance and effective legal operations.

The Director of Biostatistics will lead statistical strategy for clinical development programs, design studies, and provide statistical input for regulatory submissions while collaborating across teams.

The Administrative Assistant supports multiple teams, managing calendars, travel, expense reports, meeting logistics, and office inventory.