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方向：腫瘤、血液腫瘤、風(fēng)濕免疫
1、 Job Responsibilities /工作職責(zé)：
? Responsible for the formulation and update of SOPs;負(fù)責(zé)部門SOP 的制定與更新；
? Provide medical and scientific advice to internal partners, including but not limited to Study Design, provide strategic decision-making for clinical development plan, review the scientific/legal compliance and feasibility of the Protocol, determine the target Site and Principle Investigator, expected patient recruitment, standard of care and competitive landscape;向內(nèi)部合作方提供醫(yī)學(xué)和科學(xué)建議：包括但不限于為方案設(shè)計、為臨床發(fā)展計劃提供戰(zhàn)略決策、審查方案的科學(xué) 法律合 規(guī)性和可行性、確定目標(biāo)研究中心和主要研究者 、預(yù)期患者招募、標(biāo)準(zhǔn)治療和競爭格局；
? Provide high-level supervision on designated projects or trials from medical aspects;
在臨床試驗階段，從醫(yī)學(xué)層 面對指定項目或試驗提供高級監(jiān)管；
? Provide medical input and scientific consulting for internal team;為團隊提供醫(yī)學(xué)臨床科學(xué)咨詢專業(yè)知識；
? Establish and maintain a resource database of Medical Experts, and maintain good contact with them;
? Lead or promote medical commercialization projects, including excavating customer needs before kick-off meeting, and visiting by Medical Experts, etc.主導(dǎo)或推動醫(yī)學(xué)商業(yè)化項目，包括項目立項前挖掘客戶需求、醫(yī)學(xué)項目的專家拜訪等。
2、Personnel Management /人員管理職責(zé)：
? Determine and adjust the development direction of the Department, and be fully responsible for daily personnel management, quality and policy compliance;制定并調(diào)整部門發(fā)展方向，全面負(fù)責(zé)部門日常人員管理、質(zhì)量和政策合規(guī)；
? Coordination and cooperation with other functional departments.各職能部門之間的協(xié)調(diào)與合作。
? Job Requirements /崗位要求：
1、Education Background/學(xué)歷學(xué)歷背景背景:
? At least Master degree of Clinical medicine, excellent candidates can be appropriately relaxed;臨床醫(yī)學(xué)背景，碩士及以上學(xué)歷，優(yōu)秀者可適當(dāng)放寬；
2、 Working Experience /工作經(jīng)驗：
? At least 10 years of Clinical related experience, 3 years of medical experiences in CRO or pharmaceutical company. Management experience is preferred;
臨床相關(guān)工作經(jīng)驗10年及以上，CRO或藥企醫(yī)學(xué)工作3年以上經(jīng)驗，有管理經(jīng)驗者優(yōu)先；
3、 Skills /能力能力要求要求：：
? Familiar with GCP and other relevant rules and regulations, have knowledge on drug development process;掌握GCP等相關(guān)法律法規(guī)，了解藥物研發(fā)過程；
? Fluent English on both written and verbal;英文口語和寫作俱佳；
? Excellent communication and influence skills.溝通和影響能力俱佳。
4、Others/其他：其他：
? Deep understanding of Pharmaceutical Industry and rich clinical research knowledge;
深刻理解制藥行業(yè)，臨床研究知識豐富；
? Highly sensitive to Business, and have strategic insight to promote new Business directions from medical perspective;
高度的商業(yè)敏感性，具有從醫(yī)學(xué)角度推動新業(yè)務(wù)方向的戰(zhàn)略洞察力；