Job Roles:1. Receive, triage, review and process SAE and /Adverse event reports from various sources on time and quality standards.2. Writing narratives: Create complete, accurate and succinct narratives adhering to established processes.3. Coding terms, as appropriate.4. Ensuring reports are sent to client (submission in the client database) within agreed timelines; updating narratives when updated information is received, as appropriate; liaising with client, executing case closure, and reconciliation.5. Identifying SAEs and AEs from literature sources and processing them appropriately.6. Identifying suspect product following receipt of report; identifying reporting sources; and assessing reportability and expectedness of events.7. Prioritize cases according to regulatory and project/client requirements.8. Identify and record quality problems and bring them to the attention of Senior Team Members and Line Managers. Do a root cause of errors and understand the corrections required for cases not accurately data based.9. Review and respond to e-mails after discussion with mentors/as appropriate and attend all appropriate meetings (Quintiles and/ client).10. Complete all trackers applicable in the process.11. Code time appropriately and apply leaves after discussion with Line Managers.12. Attend and/ complete all trainings (Quintiles and client) within the specified timeline.13. Ensure integrity and completeness of data according to applicable regulations and guidelines, SOPs and project-specificguidelines.

Key roles:• Ward round with adverse drug monitoring and analysis• Antimicrobial and Prescription audits• Patient counseling & Therapeutic Intervention• Treatment chart & Medical history review