2027 Intern, Data Management

You will gain meaningful, hands-on experience supporting 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.

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.

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.
• 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.