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New Jersey Licensed Safety Specialist
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
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