Safety Data Management Intern

• Support activities tied to adverse experience case management
• Coordinate and analyze data in pharmacovigilance systems
• Enhance supporting technical systems
• Participate in process improvement activities
• Support training initiatives
• Complete and update department documentation
• Work with the Safety Data Management management team on strategic operational elements
• Collaborate with cross-functional partners and stakeholders
• Gain exposure to global adverse experience case management for drugs, vaccines, biologics, and devices

• Currently enrolled in a bachelor’s or master's degree program
• Excellent written and verbal communication skills
• Strong organizational skills
• Able to commit to full-time onsite or hybrid employment for 10–12 weeks beginning June 2027
• Strong data analysis and technical skills
• Document management skills
• Initiative, leadership, and ownership of deliverables
• Self-starter and fast learner
• Ability to multitask and work in a fast-paced team environment
• Ability to manage and independently drive projects to completion
• No visa sponsorship available

Demonstrates strong data analysis and technical skills while effectively managing documentation and supporting adverse experience case management. Capable of collaborating with cross-functional teams and driving projects to completion in a fast-paced environment.

• Data Analysis
• Pharmacovigilance Systems
• Document Management
• Process Improvement
• Communication Skills

• Data Analysis
• Technical Skills
• Document Management

• Organizational Skills
• Initiative
• Leadership
• Self-Starter
• Multitasking

• Adverse Experience Case Management
• Drugs
• Vaccines
• Biologics
• Devices

• Pharmacovigilance Systems