Moderna Therapeutics

Moderna Therapeutics is seeking an Associate Director, CMC Regulatory Science-International based at the UK site. You will develop regulatory strategies, oversee submissions, and guide cross-functional teams on CMC matters for global programs, including vaccines and oncology. The role requires leading interactions with regulatory authorities and managing multiple projects in a fast-paced environment. You will bring 10+ years in pharma/biotech with biologics CMC experience, and an MS/PhD in a

Principal Scientist, Immunogenicity and Ligand Binding AssaysApplylocations: Oxford - England: Clinical Developmenttime type: Full timeposted on: Posted Todayjob requisition id: R19340 The Role: Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.This role sits at the forefront of Moderna's clinical bioanalytical strategy, providing deep scientific expertise and hands-on leadership across immunogenicity and ligand binding assay (LBA) bioanalysis for our mRNA-LNP therapeutic pipeline. As an individual contributor, you will shape and execute phase-appropriate bioanalytical strategies that enable critical clinical development decisions while ensuring the highest standards of scientific rigor and regulatory compliance.Working closely with cross-functional development teams, you will drive regulated immunogenicity and bioanalytical activities spanning assay development, validation, sample analysis, data interpretation, and regulatory support. You will play a pivotal role in advancing innovative medicines through clinical development while leveraging modern digital capabilities and emerging analytical technologies, including opportunities to work alongside advanced data and AI-enabled approaches that accelerate scientific insight generation. Here's What You'll Do: Provide scientific and hands-on oversight of ligand binding assay (LBA)-based bioanalyses supporting Moderna's mRNA-LNP therapeutic development programs. Support and oversee the Immunogenicity function through clinical science-driven, phase-appropriate, and risk-based bioanalytical development strategies across advancing stages of clinical development. Lead and facilitate anti-drug antibody (ADA) assay and neutralizing antibody assay regulated method development, validation, and clinical sample testing activities. Ensure in-house GcLP compliance across the LBA team, systems, and procedures, maintaining rigorous laboratory practices and regulatory requirements for analytical activities through a phase-appropriate approach. Design and execute phase-appropriate clinical analytical strategies supporting development programs. Drive development, validation, and implementation of: + Cell-based assays + Immunoassays + Quantitation of translated proteins + Pharmacokinetic (PK) assays + Pharmacodynamic (PD) assays Review and evaluate raw analytical data, assay validation data, and study reports to ensure scientific integrity, data quality, and compliance with current regulatory, industry, and Moderna standards. Assess analytical performance and laboratory compliance to ensure data generated meet both scientific and regulatory expectations. Collaborate with internal and external stakeholders to support clinical bioanalytical activities throughout the product development lifecycle. Contribute to regulatory submissions and support responses to regulatory authority questions and information requests. Maintain current knowledge of emerging scientific literature, industry best practices, regulatory expectations, and evolving guidance related to clinical bioanalysis. Ensure adherence to Good Clinical Laboratory Practice (GcLP), Good Laboratory Practice (GLP), Good Clinical Practice (GCP), internal SOPs, applicable regulations, guidance documents, and relevant white papers. Apply scientific judgment and risk-based decision making to support robust bioanalytical strategies that accelerate development while maintaining quality and compliance. Partner with multidisciplinary teams to advance innovative analytical approaches and continuously improve laboratory and bioanalytical processes. The key Moderna Mindsets you'll need to succeed in the role: We obsess over learning. We don't have to be the smartest we have to learn the fastest. We act with dynamic range, driving strategy and execution at the same time at every step. Here's What You'll Need (Basic Qualifications) A Ph.D. in infectious disease, Immuno-oncology, Immunology, Cancer Biology, or related fields and a minimum of 10+ years of industry biotech/pharmaceutical experience. M.S. with extensive bioanalytical experience are considered Experience with RNA, biologics and cell therapy preferred Experience of various platforms such as ECL, Gyrolabs, reporter gene assays, DelPhia assays and other methodologies for clinical assays. Ability to effectively communicate scientific concepts, program objectives, data analysis within a matrix environment. Knowledge of GLP requirements and understanding of current industry trends and regulatory expectations associated with bioanalytical science. Experience on Watson LIMS and LabVnatage eLBN would be an advantage. A desire to make an impact as part of a high-growth, transformational companythat is Bold, Relentless, Curious, and Collaborative. Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work. That's why our global benefits and well-being resources are designed to support you-at work, at home, and everywhere in between. Best-in-class healthcare, plus voluntary benefit programs to support your unique needs A holistic approach to well-being with access to fitness, mindfulness, and mental health support Family building benefits, including fertility, adoption, and surrogacy support Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown Savings and investments to help you plan for the future Location-specific perks and extrasThe benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit to learn more about our current opportunities.Moderna is a smoke-free, alcohol-free, and drug-free work environment.Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at .

Moderna Therapeutics in Oxford is seeking a Principal Scientist for Immunogenicity and Ligand Binding Assays. This role involves overseeing bioanalytical activities, ensuring compliance and scientific integrity while facilitating innovative clinical strategies. The ideal candidate will hold a Ph.D. and possess over 10 years of relevant experience, contributing to advancing Moderna's mRNA-LNP therapeutic pipeline. The company offers a range of benefits to support well-being and professional development.

Moderna is strengthening its Harwell site and expanding bioanalytical capabilities to support our growing mRNA pipeline. As a Scientist in Bioanalytical and Molecular Assays, you will design and deliver immunogenicity and bioanalytical strategies to advance clinical programmes, working closely with multidisciplinary teams across research, bioanalysis and clinical development. You will lead development of assays (ADA, nAb, PK/PD) and ensure qualification/validation to regulatory timelines, using

The Role Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Harwell, a globally recognised centre for scientific research and innovation. Our Harwell team is expanding the bioanalytical capabilities that support our growing mRNA pipeline, bringing together exceptional scientists to advance transformative medicines for patients around the world. As a Scientist within the Bioanalytical and Molecular Assays team, you will play a pivotal role in advancing Moderna's clinical development programmes by designing and delivering innovative immunogenicity and bioanalytical strategies. Working closely with multidisciplinary teams across research, bioanalysis and clinical development, you will help generate the high-quality data that accelerates novel mRNA-derived therapeutics from discovery into the clinic while contributing to future pipeline innovation. This is an exciting opportunity to combine scientific expertise with cutting-edge technologies in a highly collaborative environment. Alongside developing robust bioanalytical capabilities, you will have opportunities to leverage emerging digital technologies and Generative AI-enabled tools that continue to transform scientific workflows, data interpretation and decision-making across Moderna's research organisation. Here's What You'll Do Design and execute phase-appropriate bioanalytical strategies supporting regulated clinical programmes. Lead the development of immunogenicity assays, including anti-drug antibody (ADA) and neutralising antibody (nAb) assays, alongside pharmacokinetic (PK) and pharmacodynamic (PD) assays for therapeutic protein quantitation. Ensure bioanalytical assays are developed, qualified and validated in line with programme timelines and applicable regulatory expectations. Develop and optimise assays using ELISA, MSD, cell culture, immunoblotting and other relevant bioanalytical technologies. Help establish and expand Moderna's internal bioanalytical capabilities to support the growing mRNA portfolio. Procure, qualify and maintain analytical laboratory equipment while preparing and maintaining Standard Operating Procedures (SOPs). Determine, qualify and control critical assay reagents to support robust and reproducible assay performance. Partner closely with Preclinical, Clinical Operations and Sample Management teams to define sample journeys and develop laboratory manuals supporting regulated studies. Troubleshoot scientific and technical issues that arise during assay development and regulated bioanalytical activities. Communicate scientific concepts, experimental findings, programme objectives and data analyses effectively within a highly matrixed global environment. Contribute to the integration of basic science research, bioanalysis and informatics to advance programmes into clinical development while helping translate clinical findings into future opportunities across Moderna's pipeline. Here's What You'll Bring to the Table PhD with at least three years of relevant experience, or an MSc with five or more years of hands-on experience in bioanalytical method development, validation and sample analysis. Equivalent combinations of education, technical training and relevant laboratory experience will also be considered. Strong knowledge of Good Clinical Practice (GCP) requirements together with an understanding of current regulatory expectations and industry trends within bioanalytical science. Expert knowledge of bioanalytical assay platforms including electrochemiluminescence (ECL), immunoassays, cell culture-based assays and related clinical assay methodologies. Hands-on experience with cell culture assays is advantageous. Experience working with RNA therapeutics, biologics and/or cell therapies is preferred. Working knowledge of translational science and the evolving competitive landscape within the mRNA field. Curiosity, adaptability and a willingness to learn new scientific concepts while challenging conventional thinking. Excellent attention to detail and the ability to manage multiple projects within a fast-paced research environment. Experience using Laboratory Information Management Systems (LIMS) and electronic laboratory notebook (eLNB) platforms is preferred. Knowledge of FDA, MHRA and global regulatory data standards. Excellent communication skills with the ability to explain scientific concepts, programme objectives and data analyses across multidisciplinary teams. This is a site-based position requiring full-time presence at Moderna's Harwell site and is not eligible for remote working. As part of Moderna's commitment to workplace safety, this role may require an enhanced pre-employment check. The key Moderna Mindsets you'll need to succeed in the role "We act with urgency; Action today compounds the lives saved tomorrow." "We prioritize the platform over any single solution." Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well-being resources are designed to support you-at work, at home, and everywhere in between. Competitive healthcare, plus voluntary benefit programs to support your unique needs A holistic approach to well-being with access to fitness, mindfulness, and mental health support Family building benefits, including fertility, adoption, and surrogacy support Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown Savings and investments to help you plan for the future Location-specific perks and extras The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit to learn more about our current opportunities. Moderna is a smoke-free, alcohol-free, and drug-free work environment. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply! Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at . - Our Mission and Vision At Moderna we are pioneering the development of a new class of drugs made of messenger RNA (mRNA). This novel drug platform builds on the discovery that modified mRNA can direct the body’s cellular machinery to produce nearly any protein of interest, from native proteins to antibodies and other entirely novel protein constructs that can have therapeutic activity inside and outside of cells. We have a clear mission to propel the field of mRNA science forward and deliver new medicines to patients and a unique vision for how to achieve this mission. Our Mission: To deliver on the promise of transformative messenger RNA (mRNA) science to bring new medicines to patients. Our Vision: To unlock the potential of mRNA by establishing an ecosystem of teams and partners that will work together to develop the broadest possible array of drugs, across diverse therapeutic areas and routes of administration, for serious diseases that are not treatable today. Third Party Staffing Agencies Moderna does not accept unsolicited resumes from any source other than directly from candidates . click apply for full job details

Associate Director, Global Regulatory Science, CMCSkip to main content Director, Global Regulatory Science, CMC page is loaded Associate Director, Global Regulatory Science, CMCApplylocations: London - England: Clinical Developmenttime type: Full timeposted on: Posted Todayjob requisition id: R19319 The Role Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.Moderna is expanding its international presence, integrating cutting-edge biotechnology within the vibrant hub of pharmaceutical innovation. We invite professionals to join us in Basel, contributing to our mission of delivering groundbreaking mRNA medicines and impacting lives worldwide.Moderna is seeking an experienced Associate Director for Global Regulatory Science, CMC. This pivotal role involves leading regulatory activities, developing CMC strategies for international submissions, ensuring compliance, and guiding product development projects. You will be at the forefront of preparing and overseeing critical regulatory documentation, directly contributing to the development of transformative medicines for patients. Here's What You'll Do Within 3 Months, You Will Develop and implement effective CMC regulatory strategies for international submissions. Start reviewing documents for submission-readiness, ensuring conformity with health authority guidelines. Begin providing regulatory guidance to manufacturing and quality teams. Within 6 Months, You Will Lead regulatory CMC discussions and interactions with health authorities. Enhance regulatory processes and procedures supporting CMC components. Support the creation and maintenance of CMC submission templates. Within 12 Months, You Will Provide comprehensive CMC regulatory guidance for various therapeutic areas. Oversee multiple programs, evaluating CMC change controls and their impact on internal programs. Lead and support all regulatory activities, delivering high-quality CMC sections of regulatory documentation. Here's What You'll Need (Basic Qualifications) BS in Pharmaceutics, Chemistry, Chemical Engineering, or closely related field is required. MS degree in Pharmaceutics, Chemistry, Chemical Engineering, or closely related field is desirable 10+ years of experience in the pharmaceutical/biotech industry, manufacturing and/or analytical focus 8+ years of experience in Biologics focused Regulatory CMC Multidisciplinary focus on certain therapeutic areas (vaccines, oncology and/or rare diseases) Strong knowledge of current EU and ROW regulations Strong knowledge of Cgmp Strong experience with CTD format and content regulatory filings Exceptional written and oral communication As part of Moderna's commitment to workplace safety, this role may require an enhanced pre-employment check Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work. That's why our global benefits and well-being resources are designed to support you-at work, at home, and everywhere in between. Best-in-class healthcare, plus voluntary benefit programs to support your unique needs A holistic approach to well-being with access to fitness, mindfulness, and mental health support Family building benefits, including fertility, adoption, and surrogacy support Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown Savings and investments to help you plan for the future Location-specific perks and extrasThe benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit to learn more about our current opportunities.Moderna is a smoke-free, alcohol-free, and drug-free work environment.Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at .

Moderna Therapeutics is seeking an Associate Director for Global Regulatory Science, CMC in London, England. This pivotal role involves leading regulatory activities, developing CMC strategies for international submissions, and overseeing critical regulatory documentation. The ideal candidate will have over 10 years of experience in the pharmaceutical/biotech industry and 8 years focused on Biologics regulatory CMC. Attractive benefits and a dynamic workplace are offered.

The role: Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is strengthening its presence in London, a global center of science and innovation. Our team drives commercial operations to bring our mRNA medicines to patients across the UK. We welcome talent ready to help transform global health. This is a high-profile, customer-facing leadership role at the heart of Moderna's UK pandemic preparedness and resilience strategy. You will lead the execution of a landmark Long-Term Strategic Partnership with the UK Government, shaping the future of mRNA-based vaccines and biomanufacturing in the UK.Operating at the intersection of strategy and execution, you will orchestrate complex, cross-functional programs while engaging senior government stakeholders to deliver meaningful public health impact. You will play a pivotal role in advancing Moderna's mission by driving delivery across R&D, manufacturing, and access to respiratory vaccines, while navigating a dynamic and evolving healthcare ecosystem. Here's What You'll Do: Lead execution of the Moderna UK government strategic plan in partnership with UKHSA and external stakeholders, ensuring delivery of all commitments under the Long-Term Strategic Partnership Serve as a primary customer-facing leader, managing day-to-day interactions with UK government stakeholders including UKHSA, Department of Health and Social Care, NHS, and the broader healthcare ecosystem Represent Moderna on the UKHSA operations board, bringing in internal subject matter experts to address questions, develop solutions, and support decision-making Provide oversight of program challenges, risks, and issues in close collaboration with government partners, ensuring transparency and effective resolution Lead and develop matrixed, cross-functional teams spanning R&D, manufacturing, policy and public affairs, market access, tender and contracts, legal, finance, regulatory, and HR Drive cross-functional collaboration to achieve program objectives and deliver external commitments within agreed timelines and quality standards Ensure alignment of messaging across internal and external workstreams, representing senior leadership perspectives where required Define and develop integrated program plans across multiple workstreams, including scope, resource requirements, milestones, roadmaps, KPIs, and budgets Establish and maintain governance frameworks to support execution, reporting, and decision-making across the program Facilitate workshops, team meetings, and planning sessions to drive alignment, execution, and documentation of strategies and outcomes Coordinate interdependencies across functions to preserve the program's critical path and ensure seamless execution Develop and maintain schedules, timelines, KPIs, and performance reports, ensuring all contractual milestones and deliverables are achieved on time Track and report progress using appropriate management tools, ensuring accuracy, transparency, and accountability Lead risk management efforts, including identification, mitigation planning, contingency development, and escalation where required Oversee development and delivery of reports tied to contractual commitments within the Long-Term Strategic Partnership Ensure robust documentation and knowledge management to support governance and future knowledge transfer Shape the external environment by anticipating emerging challenges, influencing stakeholders, and removing roadblocks across complex organizational structures Build and maintain strong, trust-based relationships with senior government officials, acting as a key representative of Moderna Operate with an entrepreneurial mindset to navigate ambiguity, seize opportunities, and solve complex challenges across both strategic and executional dimensions The key Moderna Mindsets you'll need to succeed in the role: "We act with dynamic range, driving strategy and execution at the same time at every step. We behave like owners. The solutions we're building go beyond any job description." Here's What You'll Bring to the Table (Preferred Qualifications) Well-developed interpersonal skills with the ability to communicate effectively with key stakeholders, at all levels of management Knowledge of UK government and the UK healthcare ecosystem Commercial mindset with deep customer understanding gained through experience of working with or for DHSC, UKHSA NHSE etc. Solid understanding of how a biopharmaceutical company operates experience with vaccines an advantage. Customer focus/account management and an ability to work cross-functionally Superior ability to engage with senior external stakeholders and multiple governments organizations to create innovative solutions and resolve issues. Ability to lead effectively in ambiguity and rally team around common objectives. Project Management skills with experience in design, delivery, execution and governance of project milestones. Experience with agile and lean methodologies an advantage Results focused with strong attention to detail Motivated and possessing a "can-do-it" attitude. Ability to work in a high volume fast paced environment Strong team player capable of leading by influence with experience navigating & influencing stakeholders at all levels Ability to produce and present clear, concise, and professionally written communications and presentations Demonstrated ability to apply systems thinking and analysis techniques to complex challenges Sound technical aptitude and proven ability to grasp general knowledge of multiple disciplines and technologies with superior comfort with digital tools Ability to thrive and adapt in a fluid environment and foster a strong collaborative spirit Solid judgement with ability to make good decisions Ability to influence, collaborate and align with cross-functional and matrix partnership on key program or projects, driving accountability and outcomes A desire to be part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative As part of Moderna's commitment to workplace safety, this role may require an enhanced pre-employment check. Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work. That's why our global benefits and well-being resources are designed to support you-at work, at home, and everywhere in between. Best-in-class healthcare, plus voluntary benefit programs to support your unique needs A holistic approach to well-being with access to fitness, mindfulness, and mental health support Family building benefits, including fertility, adoption, and surrogacy support Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown Savings and investments to help you plan for the future Location-specific perks and extrasThe benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great