Pharmacovigilance Associate

Job Summary

Supporting compliance functions, the fully remote Adverse Events Reporting Associate (Pharmacovigilance) will manage the intake, documentation, and submission of Adverse Events and Product Complaints identified during market research activities, ensuring timely and accurate case handling.

Key responsibilities

• Review and validate potential Adverse Events and Product Complaints against client-defined criteria
• Complete and submit client-specific reporting forms accurately within required timelines
• Maintain internal logs and documentation to ensure audit readiness and compliance with data privacy standards

Required qualifications

• Bachelor's degree in life sciences, psychology, public health, healthcare, market research, or a related field preferred
• Experience in pharmacovigilance, drug safety, research, healthcare, or quality processes (internships acceptable)
• Basic understanding of adverse events and safety reporting concepts
• Familiarity with regulatory frameworks such as FDA, EMA, or GDPR principles
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)