Safety Data Management Intern

Jobtailor; New Jersey; Hybrid; USD 25,000 - 30,000; Full time

Job summary

Jobtailor is seeking a motivated internal candidate for a 10–12 week, full-time hybrid/onsite internship in New Jersey. You will support adverse experience case management, analyze pharmacovigilance data, and help enhance technical systems.

This role emphasizes initiative, leadership, and rapid learning within a collaborative team. Ideal candidates are enrolled in a bachelor’s or master’s program, with strong communication, organizational, and documentation skills, and a drive to drive projects

Qualifications

• 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

Responsibilities

• 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

Skills

Data Analysis

Communication

Organization

Leadership

Project Management

Multitasking

Self-Starter

Fast Learner

Cross-Functional Collaboration

Initiative

Education

Bachelor's or Master's student

Tools

Pharmacovigilance Systems

Document Management Systems

Job description

• 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

Requirements

• 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

Core Competencies

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.

Highest-signal resume keywords

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

ATS Optimization Keywords

Hard Skills

• Data Analysis
• Technical Skills
• Document Management

Soft Skills

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

Industry Keywords

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

Tools & Technologies

• Pharmacovigilance Systems