Senior Pharmacovigilance Associate

Job Summary

Seeking a full-time Senior Pharmacovigilance Associate to manage day-to-day drug safety operations remotely, ensuring regulatory compliance while collaborating with internal and external teams on serious adverse events.

Key responsibilities

• Oversee daily drug safety operations with minimal guidance, ensuring adherence to procedures
• Collaborate with internal medical, data, and regulatory teams, as well as external vendors and auditors
• Manage serious adverse event reporting and ensure compliance with regulatory requirements

Required qualifications

• Bachelor's degree in a life sciences field or equivalent professional training and certification in pharmacovigilance
• 3-4 years of experience in Drug Safety or a related field
• Experience in case processing, including SAE and SUSAR reporting
• Proficiency with the ARGUS safety database, including XML generation and electronic submissions
• Willingness to be on call for after-hours and weekend safety desk coverage