New Jersey Licensed Safety Specialist

Job Summary

A company is looking for a Sr Safety Specialist to support regional and global Drug Safety Pharmacovigilance projects.

Key Responsibilities

• Manage and support Global Safety Teams, tracking pharmacovigilance activities and safety signal management
• Support clinical drug development project managers by managing safety timelines and ensuring timely completion of tasks
• Oversee vendor management, including contract tracking, budget reviews, and invoice processing

Required Qualifications

• B.A./B.S. in life/health sciences or related field
• Minimum 5 years of experience in the pharmaceutical industry, specifically in Drug Safety or Clinical Development
• PMP certification is preferred
• Experience with Clinical Trial Management and vendor management
• Working knowledge of relevant regulations and Drug Safety databases is desirable