Pharmacovigilance Associate

To support pharmacovigilance operations, the full-time remote Pharmacovigilance Associate will manage adverse event reporting, collaborate with internal and external stakeholders, and ensure compliance with regulatory requirements for investigational products. Key Responsibilities: Serve as the main point of contact for adverse event inquiries and reviews within safety and clinical databases Conduct initial reviews of SAE/AESI reports and perform quality control checks in the Argus database Assist in the preparation of safety reports for regulatory agencies and maintain documentation within the eTMF Required Qualifications: Bachelor's degree or higher in a clinical or closely related field 2-3 years of relevant experience in a biotech or pharmaceutical company 1-2 years of experience in cellular therapy, stem cell transplant, and/or oncology preferred Proficiency in the Argus safety database system Working knowledge of MedDRA and WHODrug coding preferred