Safety Specialist

• Perform and potentially oversee day-to-day Pharmacovigilance activities in a highly regulated environment
• Collect, monitor, assess, evaluate, research, and track safety information
• Collaborate with project team members, client contacts, investigators, adverse event reporters, and third-party vendors
• Participate in on-call duties for specific projects to ensure 24-hour case-intake coverage from investigative sites
• Operate in a lead capacity and assist with developing program and departmental procedural documents
• Prepare for and attend audits
• Mentor less experienced staff
• Review regulatory and pharmacovigilance publications and information sources
• Maintain medical understanding of applicable therapeutic areas and disease states
• Review cases and peer reports for quality, consistency, and accuracy
• Coordinate routine project implementation, including Clinical Trials and Endpoint Assessment Committee/Data Safety Monitoring Committee activities
• Present at client and investigator meetings
• Review metrics and budget considerations

Explore Senior Safety Specialist at Thermo Fisher Scientific. Review requirements and application details.