国产中文无码av每日更新在线观看, 亚洲天堂中文字幕一区二区三区免费, 国产口爆吞精在线观视频-黄色国产, 92福利-国内精品久久久久久99,亚洲成AV人A片不卡无码,浪潮AV无码专区,老熟女败火白浆,中文字幕日产av,色情日本免费看大片

Primary Responsibilities: 1. Responsible for ensuring global regulatory reporting compliance by execution of processes and compliance with procedures for processing safety reports originating from clinical studies, literature, hotline, regulatory feedback data, social media and/or other sources for post-marketing products. 2. Identifying and capturing accurately the relevant information of ICSRs (Including serious and non-serious cases from unsolicited and solicited origin; and literature cases, as required) in safety database in accordance with ClinChoice and/or client conventions/guidelines, SOPs and liaising with the client if applicable. 3. Responsible for medical coding with MedDRA, WHODrug or other dictionaries, and narrative writing and safety review if applicable. 4. Ensuring the timely completion and distribution of AE/SAE/SUSAR/ADR/SADR reports to Health Authorities, client and/or client’s business partners etc.. 5. Ensuring timely identification of Individual Case Safety Reports and/or relevant safety information during the monitoring of the literature. 6. Maintaining a basic working knowledge of the adverse event safety profile of assigned drugs and labeling documents or IB. 7. Requesting additional information from the appropriate sender (investigators, medical representatives etc.), as required. 8. Supporting safety database creation and maintenance if applicable. 9. Supporting documents archiving in the filing system. 10. Other ad-hoc tasks assigned by PV leadership team. Qualifications： 1. Degree in life sciences or a prior experience in PV would be desirable. 2. The minimum qualification required would be a college/bachelor degree. 3. Basic conversational skills in English required. 4. Computer proficiency, an ability to work with web-based applications, and familiarity with the Windows Professional Operating System and the MS office suite (MS Word/Excel/PowerPoint). 5. Demonstrate understanding of SOPs and relevant regulations (e.g. ICH/GCP, NMPA, EMA, FDA and E2A to E2F etc.. 6. Experience in processing safety data within Argus preferred.