Jobs at Moderna

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.

Lead portfolio governance and executive reporting for one or more operating units. Coordinate cross-functional inputs, improve governance processes and reporting, prepare executive and Board updates, integrate analytics and dashboards, manage stakeholder alignment and escalations, and support evolving portfolio operations priorities.

Manage implementation and oversight of clinical biomarker sample management across trials, including protocol review, central lab database and kit specifications, sample lifecycle tracking, quality issue resolution, vendor oversight, compliance with consent and GCP/ICH, and process/procedure development for standardized biomarker usage and reporting.

Lead and manage oncology clinical trials across phases, overseeing CROs/vendors, budgets, timelines, and compliance (ICH/GCP). Develop operational strategies, provide sponsor oversight, support inspection readiness, mentor clinical staff, and collaborate cross-functionally to ensure successful study execution and program deliverables.

The role involves leading global regulatory strategy for oncology programs, overseeing submissions, interacting with health authorities, and building high-performing teams.

Lead financial planning and analysis for Moderna's CMC function, overseeing forecasting, reporting, and data governance while driving process improvements and providing strategic insights.

Lead and support end-to-end delivery of oncology clinical trials (Phase 1-3), ensuring data quality, protocol design, site activation, safety monitoring, data review/analysis, regulatory document authoring, and stakeholder collaboration to support governance and submissions.

Lead end-to-end delivery and long-term operations of Moderna's Salesforce-based Customer Engagement Platform. Own architecture, integrations (SAP, MDM, middleware), data governance, vendor and SI management, DevOps/release processes, budgets, and omnichannel engagement enablement across commercial, medical, marketing, and service teams.

Support and improve high-throughput pre-clinical QC workflows for mRNA and LNP materials. Execute and troubleshoot analytical assays (capillary electrophoresis, LC-MS, HPLC/UPLC, RT-PCR), operate and maintain automated liquid handlers and instrumentation, analyze and document data, support deviations/investigations, and contribute to workflow automation and continuous improvement in a fast-paced research environment.

The Senior Director of Global Payroll oversees payroll operations, enforcing compliance, leading a global team, and implementing process improvements and technology integration to optimize payroll functions across multiple countries.

Lead clinical supplies planning and execution for programs/studies including demand planning, labeling/packaging, distribution, IRT UAT/supply management, cold-chain logistics, vendor oversight, KPI development, and cross-functional coordination to meet study timelines and compliance requirements.

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.

As a Sr. Bioinformatics Engineer II, you will monitor bioinformatics pipelines, ensure compliance, resolve issues, and develop documentation while collaborating with engineers for improvements.

The role involves providing strategic, scientific, and operational leadership for Quantitative Systems Pharmacology at Moderna, including developing modeling approaches and collaborating across research functions to support drug development.

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 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.

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

Apply computational biology to analyze single-cell and bulk genomics and functional datasets to study T cell biology and tumor immunity, develop reproducible bioinformatics workflows (cloud-based), integrate datasets for target and biomarker discovery, collaborate cross-functionally, and communicate results to inform oncology vaccine and immunotherapy development.

Lead architecture, implementation, and operation of cloud-based AI/GenAI platforms and data lakehouse patterns. Own end-to-end delivery: ML lifecycle (MLflow), model serving, RAG/LLM systems, vector search, CI/CD, governance (Unity Catalog), and GxP-compliant validation. Mentor engineers, define standards, integrate enterprise data (SAP), and improve reliability, observability, and cost/performance.

Lead clinical development for mRNA-based oncology programs: create and manage Clinical Development Plans, design studies and protocols, oversee execution and medical monitoring, drive regulatory interactions and submissions, collaborate cross-functionally and with external partners, mentor clinical staff, and apply innovative/digital approaches to accelerate evidence generation.