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Responsibility 1.Responsible for the finalization of non-clinical registration dossier and client communication. 負責非臨床注冊資料的定稿和客戶溝通。 2.Write or review non-clinical register dossiers (module 2.4, module 2.6, module 4 reports in CTD format)) in accordance with non-clinical guidelines. 根據非臨床相關指導原則撰寫或審核非臨床申報資料（CTD格式中的模塊2.4、模塊2.6，模塊4 報告等) 。 Qualifications 1.Be familiar with the drug rgistration non-clinical regulations and process. 熟悉藥品注冊非臨床法規和流程。 2.Be familiar with FDA/NMPA and other relevant regulatory authorities. 熟悉 FDA/NMPA 及其他相關監管機構。 3.Good command of computer skill for paper works. 熟練使用電腦進行文字編輯工作。 4.At least 3-5 years non-clinical working experiences, leading the non-clinical register dossier of several IND products, with successful approval cases. 3-5 年藥品非臨床工作經驗,主導過多個IND產品的非臨床申報，有成功獲批案例。 5.Good English in reading and writing. 良好的英語讀寫能力。 6.Pharmacy, Pharmacology/Toxicology or relevant major with at least Bachelor’s degree. 藥學、藥理毒理或相關專業，本科以上學歷。 7.Familiar with the writing of non-clinical register dossier module 2.4/2.6 and module 4 report, need to have Chinese and US IND non-clinical registration experience,the experience in non-clinical trial institutions is preferred. 熟悉非臨床申報資料的撰寫，需要有中美IND非臨床注冊經驗，有非臨床試驗機構經歷者優先 二線城市均可，homebase辦公