Lead - Clinical Literature Monitoring

Job Title: Lead Associate – Clinical Literature monitoring Department: Pharmacovigilance Location: Remote, India Knowledge and Application: Proficient in biomedical literature screening, abstracting, and indexing. Basic working knowledge of biomedical literature, pharmacovigilance, and regulatory reporting. Familiarity with information storage and retrieval systems and copyright compliance. Understanding of US and ex-US pharmaceutical regulations and adverse event reporting requirements. Key Responsibilities and Authorities Job Roles & Responsibility: Perform high-quality screening, abstracting, and indexing of biomedical literature. Develop and maintain article selection, editorial, and indexing policies in collaboration with stakeholders. Train screeners, abstractors, and internal team members. Liaise with pharmacovigilance teams to meet adverse event monitoring requirements. Assist in managing literature-related systems and databases to ensure data integrity and compliance. Collabor...