Senior Pharmacovigilance Associate

Working remotely, the full-time Senior Pharmacovigilance Associate will manage day-to-day drug safety operations, ensuring regulatory compliance while collaborating with internal and external teams to handle serious adverse events. Key responsibilities Oversee drug safety operations with minimal guidance and ensure adherence to procedures Collaborate cross-functionally with medical, data, and regulatory teams, as well as external vendors and auditors Manage case processing, including serious adverse events (SAE) and suspected unexpected serious adverse reactions (SUSAR) 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 with case processing and familiarity with SAE and SUSAR Prior experience using the ARGUS safety database, including XML generation and electronic submissions Willingness to be on call for after-hours and weekend safety desk coverage