The Associate Director will design and implement analytical systems in Clinical Operations, manage complex datasets, and provide insights for clinical study planning, collaborating with multiple stakeholders.

Lead CMC regulatory strategy for oncology at Moderna, managing a team and overseeing regulatory submissions across development stages. Engage with global authorities and enhance operational efficiency through digital innovations.

Lead and manage global litigation strategies, focusing on product liability, government investigations, and regulatory actions while advising leadership on legal risks and responses.

Lead and execute in vitro selection and screening campaigns for protein design, collaborating with computational teams, and mentoring junior scientists.

The Principal Scientist will lead computational protein design for vaccines, guiding design strategies, mentoring junior designers, and collaborating with experimental teams to advance mRNA therapeutics.

The Okta Engineer will support the IAM program through Okta administration, configuration, and enhancement of security practices, collaborating with teams to manage integrations and automations.

The attorney will oversee IP litigation strategy, manage a docket of U.S. litigation matters, and coordinate with various teams for proactive disclosures and risk management.

The PAM Senior Engineer will develop and oversee privileged access management policies, drive EPM agent rollout, collaborate with IT and business teams, manage CyberArk Privilege Cloud, and enhance PAM environment while ensuring security compliance.

The Endpoint Developer builds and automates endpoints across OS environments, develops backend services and automation frameworks, and ensures compliance and security in collaboration with multiple teams.

The GxP Endpoint Engineer manages the SCCM environment for compliance in GxP operations, overseeing deployments, patch management, and QA processes while creating documentation and collaborating with various teams.

The candidate will develop algorithms for optimizing therapeutic mRNAs, collaborate with teams on data acquisition, and communicate findings. A Ph.D. in a relevant field is required along with experience in machine learning and bioinformatics.

The Director of Clinical Pharmacology will develop clinical pharmacology plans, collaborate on studies, lead regulatory document preparation, and mentor junior staff.

The Senior Product Manager will oversee Clinical Safety and Pharmacovigilance Systems, ensuring system reliability and compliance while driving innovation and product strategy.

Provide legal support for Moderna's discovery and research, advising on collaborations and R&D contracts, and managing public health initiatives and partnerships.

Lead end-to-end technical programs for Moderna's Commercial digital initiatives: translate business needs into technical roadmaps, manage scope/schedules/budgets, coordinate cross-functional delivery, drive prioritization and reporting, mentor TPMs, and ensure compliant, scalable digital solutions across multiple geographies.

Design, configure, integrate, and support SAP ICSM capabilities for clinical trial supply planning and operations. Build BTP-to-S/4HANA integrations, enable traceability, lead technical delivery (design, testing, cutover), operate in GxP/CSV environments, and provide L2/L3 support and validation documentation while collaborating with clinical, quality, and external partners.

Lead definition and delivery of supply chain data, agentic AI, and automation roadmap. Act as product owner and hands-on architect to build data warehouses, integrations with SAP, prototypes and production AI/automation solutions, establish a CoE, and drive stakeholder adoption while ensuring GxP compliance and data governance.

Lead enterprise FP&A activities including consolidated budgeting, forecasting, long-range planning, and performance analysis. Partner with commercial, R&D, CMC, and G&A leaders to deliver management reporting, dashboards, and executive presentations, support month-end close, labor/benefits forecasting, scenario modeling, and process/tool improvements to enhance accuracy and scalability.

The Executive Director leads Moderna's Quality Assurance strategy in R&D, ensuring compliance across GCP, GLP, GCLP, and GVP. Responsibilities include governance, building a QA team, and overseeing regulatory inspections.

The GxP Product Manager will lead the development of lab informatics platforms, ensuring compliance and driving user-centric solutions that align with business needs and regulatory standards.