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The Principal Statistician leads the CMC Statistics team, providing strategic statistical guidance, mentoring, and fostering statistical excellence. Responsibilities include consultation on research questions, collaboration with cross-functional teams, contributing to regulatory filings, and enhancing platforms using Quality by Design principles. The role emphasizes driving a culture of data-driven decision-making and education on statistical tools across the organization.

The Sr. Manager, Logistics Engineering will oversee the development and implementation of cold chain logistics, ensuring compliance with regulations and best practices. Responsibilities include project management, stakeholder liaison, providing expert advice on cold chain operations, and training staff on compliance guidelines. The role also involves risk assessment and maintaining updated knowledge of cold chain requirements.

The Senior Manager of Biostatistics will oversee biostatistics deliverables for clinical studies, focusing on Moderna's infectious disease vaccine programs. Responsibilities include developing protocols, managing biostatistics activities, and collaborating with both internal and external teams to ensure project success and adherence to regulatory guidelines.

The Manager, Statistical Programming at Moderna will oversee and deliver programming for clinical trials, ensuring compliance with standards. Responsibilities include collaborating with teams, developing programs for analysis, and mentoring junior members. The ideal candidate should have relevant experience in statistical programming and knowledge of clinical trial processes, especially with SAS.

The Supervisor, Quality Control at ModernaTX will manage analytical instrumentation systems and ensure compliance with regulatory requirements. Responsibilities include overseeing lab equipment operations, supporting automation efforts, managing service provider qualification, and supervising QC personnel while fostering continuous improvement and compliance within the QC department.

As an Engineer II in MS&T, you will support technology transfer in cGMP manufacturing, ensure compliance with regulations, analyze manufacturing performance, and collaborate on troubleshooting and operational improvements. You will also provide engineering support for manufacturing equipment and maintain documentation for audits.