2027 Intern, Data Management

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 Cambridge, Massachusetts, home to our global headquarters and a center of mRNA innovation. Working closely with leading universities and research institutions, our Cambridge team advances groundbreaking science that shapes the future of medicine. We welcome talent driven by innovation and committed to improving global health. This is an individual-contributor intern opportunity based at Moderna’s Binney Street location in Cambridge, Massachusetts, from January 19, 2027 – June 25, 2027 . Applicants must be available for the full duration of the intern term. You will gain meaningful, hands-on experience supporting Data Management Leads across the clinical study lifecycle in a regulated biopharmaceutical environment. Working closely with experienced DMLs, you will contribute directly to the quality, integrity, and operational execution of clinical data through data review, documentation, testing, reconciliation, quality control, and study coordination activities. Your work will help create additional capacity for Data Management Leads to focus on study strategy, risk management, vendor oversight, cross-functional decision-making, and delivery of key study milestones. Alongside your core Data Management responsibilities, you will have opportunities to learn how emerging digital and Generative AI tools can support efficient ways of working in a highly regulated environment, while maintaining appropriate quality, data integrity, and compliance standards. Here’s What You’ll Do Partner with experienced Data Management Leads to learn and apply GxP regulations to clinical data collection. Provide operational support to Data Management Leads throughout the clinical study lifecycle. Perform hands-on clinical data review to identify inconsistencies and errors and conduct trend analysis to support data quality. Support documentation, testing, reconciliation, quality control, and study coordination activities. Adhere to Good Documentation Practices (GDP) and Data Integrity requirements to maintain accurate, complete, and inspection-ready records. Help enable Data Management Leads to dedicate greater capacity to study strategy, risk management, vendor oversight, cross-functional decision-making, and achievement of key study milestones. Complete all required training assignments in a timely manner. Contribute to special projects and continuous improvement initiatives as assigned. Build practical experience working within a regulated biopharmaceutical environment and contribute to ongoing clinical and operational initiatives. Gain exposure to opportunities for responsible use of digital and Generative AI tools to enhance productivity, learning, and operational workflows within appropriate regulated 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 behave like owners. The solutions we’re building go beyond any job description.” Here’s What You’ll Need (Basic Qualifications) Currently enrolled in a Bachelor’s or Master’s degree program in life sciences, health sciences, data sciences, or related analytical field. At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship. Here’s What You’ll Bring to the Table (Preferred Qualifications) GPA of 3.3 (on a 4.0 scale) or equivalent academic achievement. Demonstrated ability to work independently while contributing effectively within a team environment. Strong written and verbal communication skills. High attention to detail and commitment to quality and compliance. Interest in working within clinical study environment under Good Clinical Practices. A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative. Our Working Model 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. Moderna is a smoke-free, alcohol-free, and drug-free work environment. Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work. That’s why our co-op benefits are designed to support you during your time with us —at work, at home, and everywhere in between. Free premium access to meditation and mindfulness classes Subsidized commuter benefits Generous paid time off, including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown Location-specific perks and extras The salary range for this role is $20.00 - $60.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual’s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance. The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology plat