- Execute drug safety data management processes, in particular: (1) case entry, (2) medical coding, (3) narrative writing, (4) case follow-up
- Perform any other support activities as deemed necessary for the processing of adverse event reports
- Communicate with responsible departments and groups within the company and the client for the completeness and conciseness of the report
- Assume responsibility over quality of data processed and submitted to regulatory authorities, ensuring consistent, efficient and quality process to meet with client and business partner timelines
- Implement strict compliance to requirements and standard operating procedures of the company, the client and the...