A company is looking for a Remote Sr Pharmacovigilance Associate III.
Key Responsibilities
Support the creation, review, and maintenance of safety procedural documentation and the Pharmacovigilance System Master File (PSMF)
Lead procedural document development and ensure collaboration with cross-functional teams
Manage Global and Local PSMFs, including data collection, quality control, and compliance with regulatory requirements
Required Qualifications
Five or more years of experience in pharmacovigilance in operational roles
Minimum three years of experience in PV quality management and PSMF maintenance
Strong understanding of global pharmacovigilance requirements
Proficient in Veeva Quality
Bachelor's degree in life sciences, pharmacy, nursing, or equivalent health experience; advanced degree is a plus
Senior Associate • Chattanooga, Tennessee, United States