辉瑞制药有限公司<br>临床学术主管（西安）<br> 工作地点：西安<br><br>职位描述：<br>专注于指定医院络活喜产品的学术推广<br>建立与医院学术专家良好的沟通平台<br>有效执行市场部的POA策略，包括在指定负责医院的特殊项目和策略<br>制定医院年度学术支持计划和学术活动，更新和维护 CRM 系统的专家体系和目标客户<br>负责医学信息沟通专员的学术信息培训<br>与医学信息沟通专员共同达成络活喜的战略目标<br><br>背景要求：<br>良好的销售业绩和学术推广能力<br>良好的沟通能力和影响力，尤其是和KOL的沟通</p> 不限

天河区红十字会医院车陂第二门诊部<br>临床护士<br> 持有护士上岗证书，2年以上工作经验，形象气质佳，静脉穿刺技术过硬。</p> 不限天河区车陂大岗路12号

上海输血技术有限公司<br>临床技术支持<br> 1、大学本科毕业，临床医学专业<br>2、良好的沟通、语言表达能力及团队合作精神</p> 不限上海闵行区友东路500号

上海猎才商务咨询有限公司<br>高级临床监察员(职位编号:job263wt090106lb003)<br> 任职要求： <br>1、临床医学教育背景，获得博士学位； <br>2、有1-3年临床工作经验； <br>3、能经常出差； <br>4、英语熟练； <br>5、熟练的计算机运用技能； <br>6、较强的沟通表达能力； <br>7、诚恳踏实、敬业进取的个人品质；</p> 不限虹口区四川北路2261嘉兰大厦6楼B座

上海沐阳医院有限公司<br>麻醉科或临床医生(职位编号:029)<br> 1、二级甲等以上医院工作5年以上经历从事麻醉，骨外科专业，有疼痛治疗经验者优先。<br>2、具有主治医师以上职称；<br>3、沟通协调能力及亲和力佳。<br></p> 不限上海市徐汇区中山南二路555—5号，上海沐阳医院

联新国际集团<br>临床护士<br> 职位职责：<br>1、协助医师执行急、门诊、住院、出诊诊疗、处置、手术业务；<br>2、执行护理教育及社区医疗之工作；<br>3、执行医疗咨询服务；<br>4、协助配合主管机关等各项检查之工作；<br>5、参与医院相关业务之讨论及会议；<br>6、其它主管交办之事务。<br><br>职位要求：<br>1、学历/科系: 专科以上护理相关科系<br>2、资历/经验: 临床工作经验二年以上，有国外护理资历或是国内境外特需病房经验者尤佳<br>3、证书要求: 护士证书<br>4、性格特征：耐心细致、乐于与人沟通、助人、抗压性强、具有爱心、恒心<br>5、技能要求：中、英文口语沟通流利、熟练操作基本 Word、Excel等办公软件<br></p> 不限上海市长宁区延安西路937号

北京百汇鹰阁医药技术咨询有限公司<br>高级临床监察员（Senior CRA）<br> Responsibility:<br><br>-Establish and implement project plans. Assist in CRF and ICF development. <br><br>-Meet clinical trials operational and financial standards. <br><br>-Act as lead CRA and / or project manager to manage clinical trials, drive the projects progress, control quality, and provide training to CRAs <br><br>-Conduct pre-study site visits: identify study sites and investigators for projects. Negotiate fees and contracts with sites. Plan and implement patient recruitment strategies. <br><br>-Prepare and submit dossiers for Ethics Committee and Regulatory approvals. <br><br>-Conduct site initiation visits. Train investigators & study site staff on study protocol, CRF’s, GCP and other study related issues. <br><br>-Carry out routine monitoring visits. Ensure protocol compliance, SFDA, and other regulatory obligations at trial sites, verify accuracy and authenticity of clinical data. <br><br>-Ensure timely reporting of all study information. Ensure strict compliance with SAE reporting. <br><br>-Manage study medication and other trial related supplies. Ensure all unused trial supplies are accounted for. <br><br>-Conduct site close out visits. <br><br>-Maintain adequate clinical trial documentation. <br><br>-Prepare study reports. <br><br>Qualifications:<br><br>-Medical school graduate with at least 2 years of clinical research working experience, bachelor's degree or above<br><br>-Have been involved in at least 3 clinical trials<br><br>-Experience in clinical trails for global companies<br><br>-Good English in professional listening, speaking, reading and writing<br><br>-Familiar with office computer skills</p> 不限北京市崇文区崇外大街3号新世界南办公楼

上海瀛科隆医药开发有限公司<br>高级临床监查员（Senior CRA）<br> 负责具体新药临床实验的组织、实施和监查工作，确保临床试验按标准操作程序执行； <br>保证试验文件的妥善保管和归档及药品的发放回收； <br>负责受试者的随访预约；<br>协调试验各方关系；<br>向受试者介绍患者须知的内容并进行讨论。<br><br>岗位要求：<br>临床医学、药学等相关专业本科及本科以上学历；<br>3年以上临床监查及项目管理工作经验；<br>熟悉临床试验监查、SFDA法规、GCP/ICH条例；<br>有较好的与人沟通、谈判、表达能力；<br>英语、日语精通者优先。</p> 不限上海市宜山路900号科技大楼C区603室

罗氏药品开发中国中心<br>00006967 临床研究监察员Clinical Trail Monitor (PDZ)<br> Who we are:<br>At Roche, we believe passionately in what we do, and that our products make a difference in people's lives. We are a successful business that can offer exciting career opportunities to you, both locally and internationally, in a supportive and rewarding culture. We know that our people are responsible for our success and we value our employees, aiming to create a work environment where feeling valued, respected and empowered is a daily experience.<br><br>Headquartered in Basel, Switzerland, Roche is one of the world's leading research-focused healthcare groups in the fields of pharmaceuticals and diagnostics. As the world's biggest biotech company and an innovator of products and services for the early detection, prevention, diagnosis and treatment of diseases, the Group contributes on a broad range of fronts to improving people's health and quality of life. Roche is the world leader in in-vitro diagnostics and drugs for cancer and transplantation, a market leader in virology and active in other major therapeutic areas such as autoimmune diseases, inflammation, metabolic disorders and diseases of the central nervous system.<br><br>The Position:<br>1.Be responsible for project management and monitoring of assigned clinical study studies in accordance with company Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP) and local operating procedures (LOGs)<br>2. Be responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.<br>3.supports local management as well as Pharma Development Operations (PDO) goals, ability to work independently<br><br>Who you are:<br>1. At least 2 years of CRA experiences<br>2. Exposure to project management of clinical studies and experience of all stages of a clinical study are preferred<br>3. Bachelor degree in biomedical/science discipline or equivalent (e.g. BSc, Registered Nurse , BPharm)<br>4. Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures<br>5. Good command of written and verbal English<br>6. Good organization skills<br>7. Other attributes: good working and proactive attitude, value importance of teamwork</p> 不限上海市张江科苑路88号1号楼2楼人力资源部收

上海瀛科隆医药开发有限公司<br>临床监查员（肿瘤医生）<br> 负责具体肿瘤新药临床试验的组织、实施和监查工作，确保临床试验的科学性和准确性。<br><br>岗位要求：<br>三甲以上医院肿瘤医生工作经验一年以上；<br>熟悉临床试验监查、SFDA法规、CGP/ICH条例者优先；<br>有较好的沟通、协调能力和团队合作精神。<br></p> 不限上海市宜山路900号科技大楼C区603室