Pharmacovigilance Associate

Job Summary

To support compliance functions, the part-time Adverse Events Reporting Associate (Pharmacovigilance) will perform intake, documentation, and submission of Adverse Events and Product Complaints remotely, ensuring timely and accurate case handling in accordance with client requirements.

Key responsibilities

• Review transcripts and data to identify potential Adverse Events and Product Complaints, validating cases against client-defined criteria
• Complete and submit client-specific reporting forms accurately within required timelines, maintaining organized documentation for audit readiness
• Communicate with project teams regarding Adverse Event requirements and assist with training logistics or process updates as needed

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 AE/PV terminology and processes is preferred
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, and Outlook)