Massachusetts Licensed Pharmacovigilance Associate

Job Summary

Working fully remote, the full-time Massachusetts Licensed Pharmacovigilance Associate will manage the processing and oversight of serious adverse events while collaborating with various departments to ensure proper safety reporting and training implementation.

Key responsibilities

• Process and manage serious adverse events and oversee patient safety matters
• Collaborate with departments, sponsors, and investigator sites on safety information collection and reporting
• Facilitate the development and implementation of training programs for personnel involved in safety management

Required qualifications

• Bachelor's Degree in a science or related field; advanced degrees (PharmD, MD, etc.) preferred
• 2-4 years of pharmacovigilance and/or drug safety experience in a CRO, pharmaceutical, or clinical trial environment
• Proficiency with ICH Good Clinical Practice guidelines and familiarity with medical terminology and clinical research
• Experience utilizing safety databases effectively
• Proficiency in English (written and verbal)