(a) 協助就規管中藥方面與內地和海外藥品規管當局聯絡和舉行會議；
(b) 負責中成藥註冊的審核及提供相關的專業支援；
(c) 負責中成藥臨床證驗及藥物測試證明書的審核及提供相關的專業及技術支援;
(d) 協助就中成藥及中藥材有關毒性，穩定性和品質標準等編寫報告；
(e) 鑒別中藥材及檢查其品質，及向下屬提供相關的專業支援；
(f) 進行中藥材安全和品質標準的教育和宣傳工作；
(g) 協助規劃及執行中藥資源研究工作及負責處理植物標本館內的中藥標本；
(h) 協助成立,開展及營運政府中藥檢測中心轄下各實驗室及中藥標本館;
(i) 執行與中藥有關的巡查、發牌、調查、藥物警戒職務；及
(j) 負責上司指派的其他職責。

[備註：可能須輪班及不定時工作。]

(a) To assist in liaison and holding of meetings with Mainland and overseas drug regulatory authorities for the control of Chinese medicines;
(b) To be responsible for the assessment of applications of proprietary Chinese medicines (“pCm’) and to provide professional and technical support to matters relating to the registration of pCm;
(c) To be responsible for the assessment of applications for certificates for clinical trial and medicinal test for pCm and provide professional and technical support to related matters;
(d) To assist in preparing reports regarding toxicity, stability, quality specification, etc of the pCm and Chinese herbal medicines;
(e) To identify Chinese herbal medicines and assess their quality, and provide relevant professional support to subordinates;
(f) To conduct education and awareness programme on the enforcement, safety and quality standards of Chinese medicines;
(g) To assist in the planning and executing of research work on Chinese medicines resources and to handle Chinese medicines specimens for herbarium repository;
(h) To assist in the setting up, commissioning and operation of Chinese Medicines Herbarium and other laboratories of the Government Chinese Medicines Testing Institute;
(i) To undertake inspection, licensing, investigations and pharmacovigilance in respect of Chinese medicines; and
(j) To carry out any other duties as assigned by seniors.

[Remark: May be required to work shift and irregular hours.]