Supporting pharmacovigilance processes remotely, the full-time Senior Pharmacovigilance Associate will manage Individual Case Safety Reports (ICSRs), perform follow-ups, and ensure compliance with regulations while collaborating with clients and internal teams. Key responsibilities Process Individual Case Safety Reports (ICSRs) and perform follow-ups in compliance with regulations and client requirements Manage serious adverse events (SAE) and product quality complaints, including unblinding and clinical trial reconciliation Support the Pharmacovigilance and Regulatory Affairs Network Department as needed, acting as Local Contact Person for Pharmacovigilance Required qualifications Life science graduate or equivalent qualification in pharmacy, nursing, or a healthcare-related field Minimum 1 year of work experience in pharmacovigilance Advanced English proficiency (spoken and written) Strong organization and management skills, including time management and multitasking Proficient in MS Office applications
Senior Pharmacovigilance Associate in workfromhome at Unknown Company
This position is listed as full time and able to be worked remotely.