? Responsible for clinical trial supply project delivery and quality for strong financial performance & customer satisfaction, in accordance with Clinical Reach's Guidelines, SOPs and practices. 負責藥品臨床試驗支持項目的交付，并根據臨床研究準則和相關標準操作流程要求確保項目獲得優質的財務表現和客戶滿意度。

? Operational delivery and reporting of awarded studies. Project delivery is achieved through collaboration with multiple parties including but not limited to client, client's CRO/vendors, sponsor, ZP depots, partner depots, Account Managers, Proposals, Contracts, Clinical Sourcing, Global Operations, Finance, Legal and Compliance colleagues. 對所負責的研究進行運營交付和必要的報備。通過多方，包括但不限于客戶、CRO/供應商、申辦方、自有庫房、合作方庫房、客戶經理、報價、合同、臨床采購、全球運營、財務、法務及合規等部門的協作完成項目交付。

? Guidelines/SOPs Adhere to applicable company Guidelines and SOPs. Maintain good knowledge of Good Manufacturing Practice (GMP), Good Storage Distribution Practice (GSDP), Good Documentation Practice (GDP), Data Integrity Policy, Good Clinical Practice (GCP) concepts and Data Integrity Policy. 準則/標準操作流程 遵守適用的公司準則和 SOP。掌握良好生產規范 (GMP)、良好儲存派送規范 (GSDP)、良好文檔規范 (GDP)、數據完整性政策、良好臨床實踐 (GCP) 概念和數據完整性政策。

Qualifications 應聘條件

Educational Background 教育背景

? Minimum degree holder with Science or equivalent qualifications, knowledge in Clinical Trial Supply chain management 擁有理工科本科或相當學歷，具備臨床試驗供應鏈管理知識

? PMI PMP or equivalent certification holder is a plus 優先考慮PMI PMP或同等證書持有者

Relevant Experiences 相關經歷

? Effectively bilingual in English and Mandarin is a must 必須具備優異的中英雙語工作能力

? Good inter-personal and communication skills 良好的人際交往和溝通技能

? Has customer focus mindset 具備以客戶為中心的意識

? High execution and decision-making skills, including prioritization skills 高度的執行和決策技能，包括優先排序技能

? Self-motivated and resourceful 自我激勵、足智多謀

? Ability to innovate 具有創新能力

? Good coaching, mentoring and supervisory skills 良好的輔導、指導和監督技能