Leading global post-marketing case processing activities, the full-time Senior Pharmacovigilance Specialist will develop workflows, ensure compliance with regulatory standards, and manage client interactions in a remote setting. Key responsibilities Oversee post-marketing case processing from intake through reporting and closure Develop and maintain pharmacovigilance workflows and ensure compliance with Good Pharmacovigilance Practices and FDA requirements Independently manage client meetings and provide mentorship to team members Required qualifications College graduate in a scientific, medical, or clinical discipline; advanced degrees preferred Minimum of 5 years' experience in drug safety or pharmacovigilance Expert knowledge of drug safety databases and scientific principles Proficiency with MS Office applications Familiarity with regulatory standards such as ISO 9001, ISO 27001, and 21 CFR Part 11
Senior Pharmacovigilance Specialist • Carson, California, United States
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