Patient Safety Associate II

Patient Safety Associate II Key ResponsibilitiesProcess and manage Individual Case Safety Reports (ICSRs) including data entry, case assessment, MedDRA coding, narrative writing, follow-up, reconciliation, and quality checks.Support regulatory safety submissions, periodic reports, and compliance tracking to health authorities.Conduct literature searches and screening to identify adverse events, safety signals, and reportable cases.Coordinate with global affiliates on safety reporting, local compliance requirements, translations, and data exchange.Assist with regulatory support activities, product registrations, safety database updates, and regulatory intelligence monitoring.Ensure adherence to SOPs, regulatory timelines, quality standards, and client requirements.Participate in audits, inspections, process improvements, metrics reporting, and training activities.Collaborate with cross-functional teams and support client interactions as required.Skills & QualificationsBasic knowledge of Pharmacovigilance, drug safety regulations, ICH guidelines, and regulatory reporting.Good understanding of medical terminology and safety databases.Strong analytical, communication, organizational, and problem-solving skills.Proficiency in MS Office and PV systems.Education & ExperienceDegree in Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, Dentistry, or related field.4+ years of experience in Pharmacovigilance, safety case processing, or regulatory reporting preferred. #LI-REMOTE .