N1 Japanese bilingual + Pharmacovigilance

You will be responsible for N1 Japanese bilingual + Pharmacovigilance related tasks with 6 to 8 years of relevant experience. Your primary expertise should lie in Pharmacovigilance data entry, including the ability to interpret source documents, assess safety information for ICSR cases, code verbatim events using the MedDRA dictionary, and evaluate seriousness, listedness, and causal relationships of events. You should have the capability to analyze source documents from a medical perspective and present the narrative chronologically. Quality management is a key aspect of this role, involving the retrospective review of ICSR source documents and data entries, ensuring accuracy in MedDRA and drug coding, and summarizing review results efficiently. Additionally, you should be adept at managing timelines for deliverables, tracking their status, and communicating effectively with clients and global team members. Your written communication skills should be logical, coherent, and suitable for reporting statuses accurately. Your role will require fluency in N1 level Japanese along with proficiency in Pharmacovigilance data entry. The hiring process will involve screening by HR, followed by two technical rounds and a final HR round. This position has already been filled, but you may explore other relevant job opportunities in Data Entry.,