2027 Intern, Data Management

Moderna • Cambridge, MA

23h • $20 - $60 • Hybrid

About The Position

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

The intern will work closely with experienced Data Management Leads, learning to apply GxP regulations to clinical data collection and following Good Documentation Practices and data-integrity requirements. The role also provides exposure to responsible use of digital and Generative AI tools within appropriate regulated processes. The position follows Moderna’s 70/30 work model, with 70% of work in the office. The role does not offer immigration sponsorship; candidates must already have U.S. work authorization and be able to maintain it without future sponsorship. Due to export-control requirements, only individuals who qualify as U.S. persons are eligible.

Requirements

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

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.

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, inspection-ready records.
• Help enable Data Management Leads to focus on study strategy, risk management, vendor oversight, cross-functional decision-making, and key study milestones.
• Complete required training assignments in a timely manner.
• Contribute to special projects and continuous-improvement initiatives as assigned.
• Gain experience in a regulated biopharmaceutical environment and contribute to clinical and operational initiatives.
• Explore responsible use of digital and Generative AI tools to support productivity, learning, and operational workflows within appropriate 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.
• May be eligible 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