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临床协调员(上海crc实习生) 浙江我武生物科技股份有限公司 上海 2-4千/月 05-28

学历要求:本科|工作经验:|公司性质:上市公司|公司规模:500-1000人

岗位职责:1.协助完成临床试验项目的资料收集、整理和归档管理;2.协助临床试验在医院开展时的受试者筛选入组工作;3.协助试验标本的采集、处理、保存和运送工作;4.协助完成临床研究药物管理和计数,包括药物的接收、保存、分发、回收和归还,并完成相关记录;5.协助研究者填写病例报告表;6.协助研究者跟踪受试者定期随访;7.协调CRA与研究者的沟通。岗位要求:1. 本科及以上学历,生物学、药学、临床医学、护理学等相关专业;2. 有临床试验经验者优先考虑;3. 较强的独立工作能力及团队合作精神;4. 有责任心,积极进取,谨慎细致,条理性强;5. 工作积极主动,良好的沟通及应变能力,具备良好自我学习能力;

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临床专员 乐普(上海)医疗器械有限公司 上海-虹口区 6-8千/月 05-28

学历要求:|工作经验:无工作|公司性质:民营公司|公司规模:150-500人

岗位职责:1、临床前文档的准备工作。2、协助研究者进行试验管理,包括协调申报伦理,研究协议签署等。3、协助研究者进行受试者筛选、入组及随访工作。4、协助完成研究资料的收集、归档和管理工作。5、协助研究者填写病历报告表。6、协助完成临床研究药物的管理和计数,并完成相关记录。7、研究者指定的其他工作。任职要求:1、临床医学或护理等相关专业,涉外护理优先考虑,本科以上学历。2、英语四级以上,良好的英语读写及听说能力。3、较强的独立工作能力和团队合作精神。4、做事认真、细心,对工作负责。5、工作积极主动,良好的沟通及应变能力,具备良好的自学能力。工作地址上海市虹口区四川北路海泰国际大厦

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临床协调员 上海爱启医药技术有限公司 上海-浦东新区 0.8-1万/月 05-28

学历要求:大专|工作经验:1年|公司性质:合资|公司规模:50-150人

1、根据项目公众号协助研究者对受试者进行管理,包括但不限于咨询、筛选工作;2、协助研究者对受试者进行药物效果检测和健康状况检测,对受试者的用药情况进行追踪处理;3、协助研究者完成研究资料的收集、归纳和管理工作;4、及时与公司各部门进行研究项目的沟通和协调。任职要求:1、熟悉CFDA新药注册申报相关的法律法规;2、有新药临床研究项目经验及一年临床协调工作经验者有限;3、熟练掌握常用的办公软件;4、较强的沟通交流和组织协调能力。

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临床监查员 CRA 上海沃比医疗科技有限公司 上海-浦东新区 4-6千/月 05-28

学历要求:本科|工作经验:1年|公司性质:民营公司|公司规模:少于50人

1. 协助临床试验中心的筛选;? Support clinical site selection;2. 负责伦理委员会沟通并获取伦理批件;? Responsible for communicating with getting Ethics Committee approvals from Clinical Sites;3. 负责临床试验协议签订;? Responsible for getting clinical investigation agreements signed;4. 协助临床启动会安排;? Responsible for supporting kick-off meeting for the clinical investigation;5. 负责提出临床试验产品规格和数量领用申请;? Responsible for putting the demand of clinical investigation medical devices with information on specification and quantity;6. 负责临床试验产品在临床研究中心的物流(临床试验产品发放、使用、回收)跟踪; ? Responsible for logistics tracking of medical devices for use in the clinical evaluation (including the release, use and retrieval);7. 负责临床试验过程监查;? Responsible for monitoring the clinical investigation;8. 负责收集临床试验产品使用性能反馈;? Responsible for collecting operational performance feedback of the investigational medical device in the clinical investigation;9. 负责病例报告表回收,进行核查,对于遗漏和错误及时反馈给研究者,防止同类错误继续发生;? Responsible for collecting CRFs, carrying out the check on the CRFs, and giving timely feedback to the clinical investigators on omissions and errors in the CRFs to avoid similar mistakes reoccurring;10. 负责数据质疑解答的跟踪;? Responsible for follow the answer of query from Data Management;11. 负责临床总结报告研究者签字和试验中心盖章;? Responsible for obtaining the investigators’ signature and investigation centers’ seal for the clinical investigation report;12. 负责回收临床试验产品:(1)完整包装及已拆外包装但内包装完整无损的的临床试验产品经ERP申请返回、同时提交不合格评审,将临床试验产品回收;(2)已拆内包装的临床试验产品经ERP申请返回,并将临床试验产品回收;? Responsible for return with the clinical investigation medical devices: 1. For the one that has integral packaging or the inner packaging is intact, it should be applied for returning in ERP and submitted to the non-conformity review, and should be return; 2. For the one that the inner packaging has been removed, it should be applied for returning in ERP and then return;13. 负责管理临床试验资料。? Responsible for the management of clinical investigation data.任职要求:1、 本科医学,药物、生物学相关专业背景;? BA in Medicine, Pharmacy, Biology or other related field2、 0-2年 相关工作经验? 0-2 years relevant experience3、 英语良好? Native Chinese, Fluent in English4、 具备良好的组织、协调、沟通能力? Good organizational and communication skills5、 有自信。? Confidence

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临床监查员/CRA 上海宏普医疗器械有限公司 上海-浦东新区 1-1.5万/月 05-28

学历要求:本科|工作经验:2年|公司性质:民营公司|公司规模:少于50人

岗位职责:1.按要求准备伦理委员会资料和临床前期准备工作;2.开展医疗器械产品的临床研究监察工作,包括医院筛选、临床试验期内的监察、临床数据的规范、准确、合法,保证临床试验顺利进行,且符合国家的相关法律法规的要求;3.与临床试验单位、CRO公司、临床试验参与人员保持良好沟通;4.掌握试验进度,了解临床试验中出现的问题,并及时有效的解决;5.对受试医院进行实地监查,及时将访视情况报告上级。任职要求:1.2年以上医疗器械临床监查工作经验,医学、临床学等相关专业;2.熟练掌握医疗器械临床试验相关法规和GCP要求;3.良好的口头和文字表达能力,善于沟通、责任心强。

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临床监察员CRA (职位编号:02) 上海贺普药业股份有限公司 上海-浦东新区 4.5-6千/月 05-28

学历要求:本科|工作经验:|公司性质:民营公司|公司规模:少于50人

1、要求临床医学本科及以上学历,感染病学专业及感染科从业经历者从优;2、良好的人际沟通能力和执行力;具有认真负责的精神;3、主要承担乙肝新药临床试验相关事宜,包括协助临床试验文件准备、临床研究访视等。4、有临床试验经验者优先考虑。

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高级客户经理 艾康(上海)信息技术有限公司 上海-静安区 0.5-1.5万/月 05-28

学历要求:本科|工作经验:3-4年|公司性质:外资(非欧美)|公司规模:50-150人

临床医学、计算机、通信、教育、医学信息或相关专业,大学本科或以上学历;有三年以上IT应用、教育或医疗行业销售经验者,具医院系统集成销售经验者佳;有良好的客户基础;熟悉计算机、网络和相关应用 ;英文四级以上;具备良好的人际交往与沟通能力、组织协调能力,开拓市场能力;性格开朗,乐观,喜欢与人沟通,乐意助人,诚信,热忱; 工作地点:上海公司福利: 1. 周末双休 2. 带薪年假 3. 五险一金 4. 本人及子女补充医疗保险 5. 年终奖金6. 业务奖金丰厚

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新药研发部——项目经理 施慧(上海)医药科技有限公司 上海-杨浦区 0.8-1万/月 05-28

学历要求:本科|工作经验:2年|公司性质:民营公司|公司规模:500-1000人

职位描述: 1.负责生物药如重组蛋白、单抗类项目的研发管理工作,包括项目实施过程中的协调沟通、跟进与督促;2.负责项目对外合作单位的筛选、业务的联系、沟通、跟进;3.及时了解项目进程中出现的问题,对关键性问题进行决策和指导,保证项目的顺利实施;4.收集、整理课题(基金)申报信息,撰写与申请基金相关的标书,进行各类科研基金课题的申报;5.国内外药监的政策法规跟进,建立并及时更新药品注册相关政策信息库。任职要求: 1.本科学历,生物制药相关专业,一年以上工作经验,从事单抗研究方面的优先考虑;2. 熟悉药品管理及注册等法规,对药物开发及申报流程、注册法规有一定的了解;3. 有撰写与申请过相关课题基金经验的优先考虑。

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临床项目管理经理 领星生物科技(上海)有限公司 上海-浦东新区 1-2.5万/月 05-28

学历要求:本科|工作经验:5-7年|公司性质:外资(非欧美)|公司规模:150-500人

岗位职责 / Job Responsibilities:1. Manage multiple IIT studies under company’s program and policy.2. Be able to optimize project management process and SOP when needed.3. Negotiate with project related members from different function Depts. to ensure the whole process going smoothly and raise the issues in time.4. Push the program target can be delivered in time through close cooperation with functional team.5. Regular report to line manager on project progress, issues / solutions, and working plan.任职要求 / Requirements:1. Over 3-4 years of project management experience in sequencing companies or clinical trial industry.2. Strong executional ability on project management process.3. Capable to learn new knowledge and interested in precision medicine industry.4. Good communication and management experiences with multi-function Depts.5. Logical and problem solving thinking.6. At least with smooth written English would be better.

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临床助理(杨浦区域) 津熙医学科技(上海)有限公司 上海-杨浦区 4.5-8千/月 05-28

学历要求:大专|工作经验:|公司性质:民营公司|公司规模:少于50人

职位描述:1、负责接待来院孕妇进行相关项目咨询;2、协助孕妇填写知情同意书、检测申请单;3、每天工作结束后整理相关信息并录入;4、负责后续回访及完整记录回访内容;5、完成上级交办的其它相关工作。任职资格:1、年龄25—35岁;2、医药学、生物学相关专业,专科以上学历;3、具有亲和力,和较好的人际沟通能力;4、思路清晰,责任心强,做事认真、细致;5、具有相关行业工作经验优先。

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医药部研发主管(急) 上海现代中医药股份有限公司 上海 0.8-1万/月 05-28

学历要求:本科|工作经验:1年|公司性质:国企|公司规模:150-500人

招聘岗位研发主管:岗位职责:主持新产品的研究开发,实现公司的产品开发目标。具体如下:(1)收集、分析市场产品信息,进行新产品立项、设计和开发工作;(2)制定新产品研发预算和研发预算,并组织实施;(3)负责制定新产品申报计划;(4)组织建立研发信息系统;(5)为研发项目提供技术支持;(6)完成领导交付的其他任务。任职要求:(1)医药、产品开发等相关专业,本科及以上学历,2年以上相关工作经验;(2)英语6级以上,具备良好的听说读写能力;(3) 熟悉产品研发程序和产品专利申请流程;(4) 有良好的沟通能力和人际交往能力、良好的洞察力和不断开拓创新能力;(5) 工作细致、认真,良好的团队合作精神。有意者请发简历至:hr@sundise.com

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项目经理 Study Manager 缔脉生物医药科技(上海)有限公司 上海-浦东新区 1-2万/月 05-28

学历要求:本科|工作经验:5-7年|公司性质:合资|公司规模:50-150人

Position SummaryResponsible for simultaneous delivery of the operational aspects of a single/multicenter clinical studies from protocol development through database release to ensure high quality, timely and cost effective conduct of the clinical trials. Ensure the study conduction in accordance with ICH-GCP, local regulatory requirements, and the Standard Operating Procedures (SOPs) of Sponsor and /or dMed. The Study manager also contributes beyond database release to support effective study reporting and close-out; submission activities; and audits/inspections, as appropriate. He/she achieves this purpose by thoroughly understanding protocol and actively managing the activities and deliverables of all study conduct.The degree of responsibility accorded to a Study Manager or Senior Study Manager will reflect their level of experience and contribution that they can make to the project.Key Responsibilities Across Entire Study:- Keep good communications with sponsor and provide regular report on the study progress, and escalate the issue with action proposal when necessary; Study overall project management, status tracking and proactively anticipate and resolve issues.- Actively manage the activities and deliverables of sponsor and all study partners (Investigator sites, site management functional lines, clinical supply, sub-contractors) to ensure timely delivery of quality data on specific studies- Effectively manage and lead project team to deliver key clinical operation milestones for serviced studies- Oversee site management functional lines to ensure that protocol and monitoring plan are consistently and appropriately implemented across clinical sites. Collaborates with the sites and site management functional lines to ensure that they are provided with the information to effectively contribute to the study- Proactively identify and resolve study operation-related issues as they arise- Ensure the clinical study operations to meet the time, quality & cost targets consistent with the plan-reached agreement with sponsor- Responsible for the studies to be conducted in compliance with ICH-GCP, relevant SOPs, and local regulatory requirements; Responsible for inspection readiness for all aspects of the study conduct- Share best practices across the organization to ensure cross-line standardization- Study Start-Up    - Feasibility, site selection and study budget- Responsible to guide or lead CRAs to conduct both protocol and site feasibilities within a required timeframe and provide input to the study management components of the protocol- Ensure appropriate site selection for a specific study- Produces study level ICD, as appropriate- Provide input to generation of a study budget plan provided to the client.   - Data Management and Programming Interactions- Support programing, data management to ensure set up of data capture tools (CRFs and EDC system, diary cards, questionnaires, translations etc.) to ensure completion within project deliverable timelines- Overall responsible for ensuring the study has efficient and effective data flows (for all types of study data, including SAEs, endpoints, patient diaries, lab data, etc.)   - Site Selection and Start-up- Develop study level subject recruitment and retention strategy or plan, including study start-up timeline; oversee implementation of plan, including site-level plans, subject recruitment and retention strategy or tools, and advertising materials- Oversee sites and site management to ensure site readiness (Clinical Site Agreements, Ethics Committee approvals, HGRAC approvals and to meet other regulatory requirements, e.g. clinical registry)  - Training and Investigator Meeting (as needed)- Develop the Monitoring Plan; ensure CRAs, sites and other site management functional lines are trained on Protocol-Specific aspects of the Study Monitoring Plan.- Work with Clinician to ensure that site management functional lines are provided with appropriate training in both the protocol and therapeutic area knowledge- Drive and/or contribute to investigator meeting strategy/agenda, responsible for overseeing implementation by the project team, and review meeting materials- Facilitate and present at investigator meetings, as required by sponsor  - Drug Supply- Collaborate with sponsor supply line to develop and complete of the Request for Clinical Supplies- Work with sponsor’s supply line to ensure that clinical trial drug supplies are ordered, produced, labeled and supplied in a timely manner- Clinical Study Conduct  - Subject Recruitment and Retention- Manage protocol-level subject recruitment and retention and take action to ensure to reach timeline. Use trial projection and tracking metrics as tools to monitor and actively manage the delivery of project team’s goals.  - Quality & Compliance Management- Periodically review protocol deviations and collaborate with clinicians to manage protocol deviations according to dMed SOPs.- Work closely with project team to ensure data quality requirements are agreed to and met, prior to reporting.- Perform required activities to identify issues and take CAPA in a timely manner. Ensure the sufficient documentation.- Work with the internal quality control, internal / external Quality Assurance and site to ensure high quality of trial. Coordinate with site audit or inspection (e.g. CFDA certification renewal inspection) if any and ensure the CAPA completion with the required timeframe.  - Other related activities- Ensure the drug supply (including resupply) process timelines, risks and issues are handled in a timely manner. Ensure investigational drug logistics and drug countability at site to meet the requirements per protocol.- Work closely with the data management function to ensure data entry, query resolution at the protocol level. Take actions to ensure the milestone of data management, data entry, data cut-off, interim analysis, data cleaning, database lock- Vendor management and oversight if any sub-contractor is involved.- Well manage and control the study budget, and keep communication with sponsor if the budget needed to be adjusted- Clinical Study Close-out- In close partnership with the sites and site management functional lines to ensure site closeout activities including the self-assessment per regulatory requirements are completed,- Responsible for the collection and consolidation of the Protocol Deviation Logs.- Accountable for study close out; support GCDS in database lock and release activities, ensuring all timelines and quality goals are met.Education and Key Competency RequirementsProfessional Experience & Education Requirement- Minimum Medical or pharmaceutical education background or other life science degrees (or equivalent); experience in clinic practice is preferred- Minimum 5 years of experience in clinical trials as CRA, at least 1 year involved in project management or equivalent, and present excellent performance and good potential to be a study manager- Good working knowledge of GCP guidelines and good sense to regulatory requirements- Proficiency in Basic Microsoft Word and Excel and familiarity with use of database- Broad knowledge of drug development process, and good relationship with investigators- For a Senior Study Manager, shall possess the mature capabilities of Study Manager. Capable and experienced in handling complex or difficult situations or projects to meet study goal. Has profound knowledge and capability to mentor or coach to junior & new members.Key Competency Requirement- Organizational commitment and result Oriented- Self-awareness and self-motivated- Well-developed of communication (Chinese & English), presentation, and interpersonal skills- Teamwork and collaborative working attitude- Demonstrate thought leadership and innovative approach contributing to project outcome- Facilitation and influence skills with multiple parties involved- Project leadership and management skills with proven record; Capable to plan and prioritize to manage competing objectives- Strong problem solving and consultation skills Resilient in changing business environment, and able to drive and implement changes effectively and positivelyImportant Note: 'Salary range' in the job requirement is just for reference. The salary will be defined after full evaluation of the candidates through test and interview. 备注: ‘职位月薪’ 仅供参考,具体薪资和福利将根据候选人经验和能力综合评定。

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临床专员 上海启功医疗科技有限公司 上海-松江区 6-8千/月 05-28

学历要求:本科|工作经验:3-4年|公司性质:民营公司|公司规模:少于50人

岗位职责(职位偏技术,公司提供完善的培训机制,统一培训上岗):1、技术支持(1)负责公司产品的临床手术跟台或提供相关跟台支持。(2)解决技术问题(包括随访中遇到的问题)(3)对产品进行随访,定期拜访客户,保证数据资料的完整性和准确性(4)收集、分享病例。2、市场定期从技术层面拜访客户,负责客户的管理、开发和维护,了解客户的需求,并从产品优势和竞争信息等方面进行销售。任职要求:1、本科以上学历,医学相关专业,临床医学专业优先(有相关血管介入工作经验者可适当放宽到大专学历);2、三年以上相关工作经验,有血管介入类产品工作经验者优先考虑;3、执行力强,积极服从和配合上级领导布置的任务并独立完成;4、具有出色的沟通协调能力和谈判技巧,能够独立处理突发事件,有团队合作精神;我们提供:完善的培训机制有竞争力的薪酬体系;完备的五险一金职位晋升空间

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产品专员(临床) 上海西贝电子科技发展有限公司 上海-金山区 4-5.5千/月 05-28

学历要求:大专|工作经验:2年|公司性质:民营公司|公司规模:50-150人

岗位职责:1、负责对销售人员、渠道及客户进行康复培训和临床操作指导;2、负责在市场活动中进行产品讲解、演示;3、部分市场推广工作;4、负责完成上级安排的其他工作。任职资格:1、年龄22-35岁,性别不限;2、康复治疗、运动康复、市场相关专业,专科以上学历;3、医疗康复器械行业或相关行业1年以上临床康复或市场推广工作经验;

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临床医学专员 上海斯丹赛生物技术有限公司 异地招聘 10-15万/年 05-28

学历要求:本科|工作经验:|公司性质:民营公司|公司规模:50-150人

主要职责:1、根据试验方案、SOP和GCP的要求进行研究中心筛选、启动、监查和关闭访视;2、通过规范的监查过程,保证临床试验按照国家GCP要求和试验方案进行;3、对临床试验管理的相关活动进行记录并存档;4、检查病例观察表(CRF)中数据的合法性、准确性和完整性;5、监督试验的进行情况,保证试验资料的完整性和正确性,并确保临床试验按计划完成;6、负责相应研究中心的研究财务管理;7、试验用药物和物品的正确保管、发放和使用;8、负责协调公司与各临床试验基地的关系,处理临床研究中心出现过的各种问题;9、完成项目组分配的其他工作。任职资格:1、拥有医学背景,临床医学或者相关专业;2、具有极强的执行力、责任心、思维活跃,具有创新及团队合作精神;3、具有国内中大型企业或中外合资企业临床监察经验者优先;

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项目研发人员 盟科医药技术(上海)有限公司 上海-浦东新区 20-30万/年 05-28

学历要求:|工作经验:|公司性质:外资(非欧美)|公司规模:少于50人

任职资格:1、临床医学、基础医学、药学、生物等相关专业,本科以上学历;2、具有1年以上的新药研发经验或临床试验CRO公司CRA、CRC的工作经验3、熟悉SFDA药品研究的相关法律法规,熟悉GCP及临床试验具体流程和相关法规者更佳4、诚信、勤奋、认真、仔细,具有良好的职业道德,有较强的责任心及团队合作精神5、具有良好的沟通和协调能力岗位职责:1、 协助完成公司在研项目的相关工作。2、 协调各CRO公司及临床试验相关研究中心的有关工作,以确保在研项目如期完成。3、 协助临床试验的准备、启动、实施和监查管理工作,确保所有试验严格按照国家GCP要求和试验方案准时、优质的进行,协调组织研究者会议及相关会议等。4、 核对临床试验原始数据及相关过程,确保临床试验数据科学可靠并及时收集,并确保病例报告表记录准确、完整。5、 协助进行临床试验及在研项目的相关管理,协调试验各方关系,与合作单位及研究者保持良好的合作关系。

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临床监查员CRA 北医仁智(北京)医学科技发展有限公司 上海 4.5-6千/月 05-28

学历要求:大专|工作经验:2年|公司性质:民营公司|公司规模:150-500人

岗位职责:1.为三甲医院科研工作提供支持;2.对临床试验管理的相关活动进行记录并存档;3.核查病例报告表(CRF)中数据的合法性、准确性和完整性;4.发放和回收药品/器械及临床试验的相关资料;5.各研究单位专家的关系维护;6.根据GCP和相关法规以及公司的SOP启动、监查和结束临床试验。 职位要求:1.临床医学或药学及相关专业专业本科以上学历;2.参加GCP、SFDA培训优先;3.有CRA经验优先;4.熟悉有关临床试验最新法规、制度;5.优秀的英语写作及口语表达能力;6.熟练使用Office等办公软件,如 MS Excel,Word,Power Point, Outlook;7.有临床医学数据管理、临床项目研究及临床工作经验者优先考虑;8.工作积极主动,具有良好的团队合作精神及一定的项目管理能力;9.可短期出差者,优先考虑。

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临床监察员 兴安药业有限公司 上海-浦东新区 6-8千/月 05-28

学历要求:本科|工作经验:1年|公司性质:外资(非欧美)|公司规模:50-150人

岗位职责:1、负责监查临床研究质量、跟踪药品的临床使用情况及临床试验工作协调;2、收集、分析药品临床数据,保证试验数据的及时、规范和准确录入;3、与研究者及研发人员沟通,确保临床试验符合规范;4、保持与研究单位和相关专家的良好沟通和协调,发现并及时地协调解决临床试验过程中出现的问题。任职要求:1、临床医学或临床药学:本科及以上学历,药学:硕士学历;2、善于与各种不同类型的客户进行交往,并能建立起良好关系的能力;3、能适应出差;职能类别:临床研究员关键字:临床监察员 临床研究 CRA

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临床协调员 上海安必生制药技术有限公司 上海-徐汇区 0.8-1万/月 05-28

学历要求:本科|工作经验:3-4年|公司性质:民营公司|公司规模:少于50人

岗位职责:1、联系临床机构,协调临床试验或生物等效试验合作模式、合同报价等2、参与临床试验方案、研究者手册及相关文件的制定;3、联系CRO完成培训相关医师、护师及试验相关人员试验方案;4、联系CRO完成最终的临床试验总结报告;5、协助注册部门整理注册所需材料; 任职要求:1、医药相关专业本科或以上学历;2、具有两年以上的相关工作经验;3、能应用英文读写、熟练应用相关工作软件;4、较强的对外沟通协调能力和语言表达能力;5、具有较强的独立工作能力和团队协作精神

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Clinical Research Coordinator (CRC, 临床研究协调员) 上海切尔西医药科技咨询有限公司 上海 3-4.5千/月 05-28

学历要求:本科|工作经验:无工作|公司性质:民营公司|公司规模:50-150人

Responsibility: - To assist the site investigator to deliver high quality patient data in accordance with ICH/CFDA-GCP and as required by the SOPs and study protocol; - To participate in the recruitment and screening of research patients; - To be responsible for use of computer applications and other technology to enhance the efficiency of the workflow in study activities including data collection and query resolution; - To collect, prepare and submit of regulatory documents as per required by the site EC; - To attend site initiation meeting; - To prepare the documents for study monitor site visits; - To assist investigator in obtaining proper written consent from each study participant according to the requirement; - To perform functions necessary for completion of sponsor protocols including scheduling, patient enrollment, medical histories, clinical assessments, laboratory-phlebotomy and processing, diagnostic studies, dispensing of investigational medication and overall organization and logistics of study visits; - To complete and correct case report forms ensuring accuracy of all records connected with each research patients; - To assist the investigator to report and record all adverse events according to GCP Guidelines and the request of sponsor; - To maintain accurate record of all study supplies including lab kits, medications and other items dispensed to patients; - To maintain close contact with sponsor concerning patient enrollment, scheduling, dosing/dispensing, abnormal laboratory values and adverse events; - To ensure a smooth communication through the studies between the site investigator and Project team. Provide weekly timesheet to sponsor project team members; - To update the TMFs and ensure the accuracy and completeness of TMFs; - To perform other duties as required. Requirements: - Bachelor or above Degree in Medicine or Nursing is a MUST; - Familiar with hospital environment; - Excellent communication skills with doctors and patients; - Detailed orientated; - Organizational skills; - Ability to multi-task; - Can work under pressure; - Doctor or nurse who has oncology experience and is interested in clinical research is preferred.

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