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Lead regulatory project management activities for global drug development, ensuring effective operational support, team collaboration, and compliance with health authority requirements.

Lead computational chemistry efforts for drug discovery, providing expertise in molecular design, mentoring junior members, and collaborating across teams.

The Translational Sciences Lead - Immunology drives research on plasma-derived therapies, managing projects, developing biomarker strategies, and collaborating across functions.

Lead digital transformation strategies across manufacturing sites, develop and implement strategic plans, and enhance operational performance through Industry 4.0 capabilities.

The Senior Validation Engineer will write validation documents, execute qualification protocols, analyze validation data, and ensure compliance with FDA standards in pharmaceutical manufacturing.

Manage analytical release and stability testing for clinical products, review GMP data, and author regulatory sections while ensuring compliance.

The Senior Principal Pharmacovigilance Scientist is responsible for leading pharmacovigilance activities, ensuring safety data compliance, and collaborating with cross-functional teams for both developmental and marketed products.

Manage statistical input for Marketed Products Development projects, collaborate on designs, perform statistical analyses using R and MATLAB, and lead process improvements.

The Sr. Director leads the pricing strategy and contracting for US Oncology, overseeing market access analytics and compliance, while managing cross-functional teams and guiding senior leadership decisions.

The Associate Manager, Data Validation Engineer oversees clinical trial deliverables, ensuring data validity through programming, reconciliation, and compliance with standards.