Pharmacovigilance Associate II

Bristol Myers Squibb seeks a Pharmacovigilance Associate II in Warsaw to support safety management operations within the R&D organization. The role involves coordinating pharmacovigilance activities, mentoring junior associates, and managing complex workstreams across global drug development projects.

Responsibilities

• Support Safety Management Teams by coordinating cross-functional activities and documenting decisions and action items
• Manage signal detection activities including scheduling meetings, generating reports, and conducting literature searches
• Administer SharePoint Online and electronic document systems for assigned product portfolios
• Execute clinical safety program activities including protocol tracking and health authority query management
• Mentor Pharmacovigilance Associate I colleagues and provide subject matter expert training and support

Requirements

• Bachelor of Science in life sciences or equivalent scientific qualification
• Minimum 3 years professional experience in health science or life sciences fields
• Minimum 2 years pharmaceutical industry or academic experience
• Strong understanding of global pharmaceutical drug development and drug lifecycles
• Demonstrated ability to mentor other employees
• Project or program management experience preferred