2027 Intern, Data Management

ModernaTX • Cambridge, MA

9d • Hybrid

About The Position

This is an individual-contributor internship based at Moderna’s Binney Street location in Cambridge, Massachusetts, running from January 19, 2027, through June 25, 2027. Applicants must be available for the full internship term. The intern will support Data Management Leads across the clinical study lifecycle in a regulated biopharmaceutical environment, contributing to the quality, integrity, and operational execution of clinical data through data review, documentation, testing, reconciliation, quality control, and study coordination activities.

The intern will work with experienced Data Management Leads and gain practical experience applying relevant regulations and working with clinical study data. The role also offers exposure to responsible use of digital and Generative AI tools in regulated workflows, with appropriate attention to quality, data integrity, and compliance. The position is based on Moderna’s 70/30 work model, with an emphasis on in-office collaboration. Moderna is unable to offer immigration sponsorship for this role, and candidates must meet the stated U.S. work authorization and export-control eligibility requirements.

Requirements

• Currently enrolled in a Bachelor’s or Master’s degree program in life sciences, health sciences, data sciences, or a related analytical field.
• Available for the full internship term from January 19, 2027, through June 25, 2027.
• Must already hold U.S. work authorization and be able to maintain it without future sponsorship.
• Must qualify as a U.S. person under applicable export-control requirements (citizen, permanent resident, asylee, or refugee).

Nice To Haves

• GPA of 3.3 on a 4.0 scale or equivalent academic achievement.
• 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 in a clinical study environment under Good Clinical Practices.
• Desire to make an impact at a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Responsibilities

• 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.
• Review clinical data to identify inconsistencies and errors, and conduct trend analysis to support data quality.
• Support documentation, testing, reconciliation, quality control, and study coordination activities.
• Follow Good Documentation Practices and data integrity requirements to maintain accurate, complete, and inspection-ready records.
• Help enable Data Management Leads to focus on study strategy, risk management, vendor oversight, cross-functional decision-making, and study milestones.
• Complete required training assignments in a timely manner.
• Contribute to assigned special projects and continuous improvement initiatives.
• Gain practical experience in a regulated biopharmaceutical environment and contribute to clinical and operational initiatives.
• Gain exposure to responsible use of digital and Generative AI tools to support productivity, learning, and operational workflows within regulated processes.

Benefits

• Free premium access to meditation and mindfulness classes.
• Subsidized commuter benefits.
• Paid time off, including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown.
• Location-specific perks and extras.
• Potential eligibility for an annual discretionary bonus, other incentive compensation, or an equity award, subject to plan eligibility criteria and individual performance.

What This Job Offers

• Job Type: Full-time
• Career Level: Intern
• Education Level: No Education Listed