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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 5-7千/月 11-18

学历要求:本科|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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静安嘉里中心-500强外资医药公司-Medical Consultant 北京外企德科人力资源服务上海有限公司 上海 1-1.5万/月 11-18

学历要求:|工作经验:|公司性质:合资|公司规模:1000-5000人

KEY ACCOUNTABILITIES:? Entertain remote scientific communication with HCPs? Participate in Sanofi China sponsored regional events on given occasions, communicating medical information,? Contact / connect with doctors through remote detailing platform, phone, SMS, email, WeChat… Multi-channel approach to maximize the number of connections with HCPs? Entertain quality discussions with the contacted doctors on medical-related general knowledge (Sanofi product, therapeutic area, disease state; trainings)? Answer questions, identify and overcome objections? Follow up on contacts,? Develop by these means excellent relationships with the doctors in the responsible territory.? Work closely with BU on the field? Receive and follow-up on field force medical related requests for customer,? Obtain customer information, preferences, needs,? Share with field team to increase respective customer knowledge,? Complete records of interactions.? Work in full compliance with company policies and guidelines, including but not limited to Sanofi Code of Conduct, Good Promotional Practice Guidelines. Ensure all product-related information is in-label information.JOB-HOLDER ENTRY REQUIREMENTS:Education:Medical background (pharmacist or doctor degree)Experience & knowledge:? At least 2-4y clinical practice, or? Life science industry experience in marketing, medical, or sales,? Previous experience in a customer support role/ Knowledge of customer service practices and principles? Experience in digital or phoning experience environment is a plus.? Proficient in relevant computer applicationsCore competencies:Remote Detailing? To provide services to customers as they move among communications channels — including social media and community forums? To deliver, push the appropriate business service, content to determine the next best action, information or process with which to engage the customers.”? To understand the customer journey including digital journey to help focus on operational efficiency and service strategies.? Seize customers opportunities when they arise /Build sustainable relationships and engage customersHCPs interaction? Strong communication skills and be able to identify and resolve problems/ Ability to handle stressful situation appropriately? Strong phone and verbal communication skills with active listening/ Customer focus and adaptability to different personality types? Obtain client information by telephone calls; interviewing clients; verifying information.? Document all calls informations according to standard operating procedures – Recognize, document, and alert the management team of trends in customer calls – Follow up customer calls where necessary dentifying customers’ needs, clarify information, research every issue and providing solutions and/or alternatives? Managing large amounts of inbound and outbound calls in a timely mannerSkills? Digital appetence , knowledge? Computer / digital savvy/ be familiar with common word-processing and spreadsheet programs,? Maintain and update database by entering customers information./Keep records of conversations in our call center database in a comprehensible way/ Familiarity with CRM systems and practices? Following communication “scripts” when handling different topics? Meet personal/team qualitative and quantitative targetBehaviour? Persuasive, tenacious, positive, energetic,? Good team spirit, /Open, curious, willing to go outside and meet external world / customers.

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Senior Clinical Project Specialist 雅培贸易(上海)有限公司 上海-黄浦区 11-18

学历要求:本科|工作经验:2年|公司性质:外资(欧美)|公司规模:500-1000人

Primary Job FunctionDescribe in 3-4 short sentences the responsibility and authority of the job.1. Clinical operational activities for Affiliate sponsored study2. Key contact person for Global sponsored study3. Quality Management and Compliance4. Support business development in New Product Introduction processCore Job ResponsibilitiesList the primary tasks and/or activities this job performs on an ongoing basis.- Affiliate sponsored study:? Key internal and external contact person of affiliate sponsored studies to support the project leader? To track the study progress in a timely manner, organize regular project review meetings, propose action plan to the project leader, and follow up; to distribute regular study progress report? To work with study physician and project leader and Affiliate Safety Representative on essential study documents, coordinate to get approval? Key contact with global team to have teleconference, coordinate global approval process? Update study information in internal study tracking system, register the study in external website? Working with external partner such as CRO project manager on study progress tracking, resource allocation, contract sign, and organize / deliver training to CRO team? Responsible for study document archiving and management? Quality control activities for specific study such as co-monitoring and site visits- Global sponsored study: to be coordinator to provide local support and as key contact person- Quality Management and Compliance? Ensure all clinical research activities follow Abbott policy, SOPs, OEC, ICH&GCP and local regulations? Interpret SOPs of clinical research activities to internal team and external partners? Participate to prepare internal audit or external inspection? Involve to develop and implement quality management system on clinical research, such as local SOP, working instruction and internal processes- Support business development in New Product Introduction processMinimum EducationIndicate the minimum education level to perform this job.- Bachelor degree or above in Clinical Medicine, Pharmacy, Biology, Chemistry, Pharmacology or related life sciencesMinimum Experience/Training RequiredIndicate the minimum experience and/or training required to perform this job.- Industry experiences: A minimum of 2 year experience- Position experiences:At least 2 years experiences of clinical researchHaving experiences in CROs or multinational phamarceutical company- Language Skills:Fluent English in reading, writing and oral communication, able to lead regular TC with global clinical study team- Computer Skills: Microsoft Office software- Certificate Required: GCP training

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临床专员 上海锐植医疗器械有限公司 上海-闵行区 5-8千/月 11-18

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

1、临床研究(试验)用相关资料的撰写(方案、说明书、研究者手册等);2、组织临床研究的实施(制定计划、实地监查、进度跟踪、协调解决);3、组织启动会,总结会,整理临床研究相关资料并及时上报;4、支持和配合公司进行注册资料准备及取证、续证等工作;5、工作认真,性格开朗,善于沟通,能与客户配合保证林场试验实施。

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临床监察员 爱乔(上海)医疗科技有限公司 上海-浦东新区 6-8千/月 11-18

学历要求:|工作经验:2年|公司性质:民营公司|公司规模:少于50人

作为临床监察员,你需要:1.筛选临床单位;2.伦理申报、合同签署及临床药理机构沟通协调;3.临床病例的入组的促进及监查;4.配合并协调CRC和或CRO公司开展工作;5.确认所有数据的记录与报告的正确完整,所有病例报告表填写正确,并与原始资料一致;6.核实试验用器械按照有关法规进行供应、储藏、分发、收回,并做相应的记录;7.确认所有不良事件均记录在案,严重不良事件在规定事件内作出报告并记录在案;8.相关文档管理。我们希望你是:1.在工作态度上:热爱本职工作、做事积极主动、不断学习进步、勇于承担压力;2.具备团队精神:强大执行力、听从指挥、行动一致、目标坚定;3.拥有的专业技能:-医药相关专业本科及以上学历;-有2年以上临床试验监察经验,经历过临床试验的所有环节;-能适应短期出差。

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临床监查员 施慧(上海)医药科技有限公司 上海-杨浦区 0.8-1万/月 11-18

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.具体负责公司临床项目的计划、开展和管理、协调等;2.协助设计、编写、制作临床试验方案和CRF的设计、研究者手册与试验相关资料;3.协助开展研究单位的调研筛选、协议谈判,召开临床试验各阶段会议,准备临床试验样品、资料及随机物品;4.负责临床试验的实施和监查工作,跟踪协调,确保研究者按照方案、GCP、SOP等相关要求进行试验,确保试验符合伦理要求、试验数据科学可靠并及时收集,确保研究中心按照时间表完成病例;5.按照检查计划定期对研究中心进行实地监查,并在规定的时间内完成监查报告,同时将访视的详细情况报告上级,使上级随时了解试验执行过程中的情况,及时发现和改正存在的问题;6.协助上级完成产品立项阶段的临床试验工作评估,与临床医院及相关临床试验员保持良好的关系;7.记录报告临床试验及不良事件与SAE;8.负责临床试验相关文件的备案、归档和管理;9.能独立完成领导安排的任务。任职资格:1.本科及以上学历,1年以上临床研究工作经验,医药、临床相关专业;2.掌握GCP及临床试验法规,熟悉临床试验方案和研究流程;3.良好的沟通能力,良好的领悟能力,良好的执行能力,良好的解决问题能力。

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Project Manage Assistant 欧陆生物科技(上海)有限公司 上海-静安区 0.8-1万/月 11-18

学历要求:大专|工作经验:|公司性质:外资(欧美)|公司规模:少于50人

Key Accountabilities1.Support of a group of Project Managers in performing their role.2. Maintain and version control of electronic and paper study files to a single location to ensure they are up to date, accurate and immediately available.3. Minute meetings in client ready format, obtain approval from PM for circulation and distribution4. Collate project tracking reports that may be required by the Project Manager.5. Document client interactions and expectations from various sources (verbal, email, sales, meetings, etc) in accordance with PM.6. Distribute and follow-through Project Management related communications or materials to internal stakeholders or sponsors in a timely and professional manner.7. Schedule and control Team calendars and filing systems (incl. internal and external archives).8. Support senior managers as requested.Requirement:1. 2 years in a similar role/job function e.g. as an Administrative Assistant2. Experience in project or service related industries a plus (professional firms, etc)3. Diploma in administration or secretarial studies.4. Certificate or degree in healthcare/life sciences or business would be an advantage.5. A proven track record of successful internal customer-service and strong stakeholder focus, driven by quality and speed.6. Excellent communication and organization skills, able to accurately handle multiple priorities.7. Energetic, enthusiastic person with a flexible and dynamic work ethic.8. Fluent in English, other languages of operating facility of advantage.8. Prolonged sitting or usage of computer systems (>75% time).

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临床协调员 上海景腾医药科技有限公司 上海-杨浦区 5-7.5千/月 11-18

学历要求:大专|工作经验:1年|公司性质:民营公司|公司规模:少于50人

任职要求1. 具有大专以上学历(含大专学历);2. 具有医学、药学或护理学教育背景;3. 了解药物临床试验工作流程,喜欢从事临床科研工作;4. 具有踏实敬业的工作态度,良好的沟通能力,较强的独立工作能力;4. 具有较好的英语写作及口头表达能力,熟练使用计算机办公软件;5. 有责任心,积极进取,谨慎细致,条理性强,具有良好的团队合作精神。岗位职责1. 为三甲医院科研工作提供支持;2. 与研究团队密切合作,确保研究高效率、高质量、按时开展;3. 根据CFDA法规要求,进行临床试验项目的管理和质量控制;4. 与机构、伦理委员会和申办方等研究相关人员及时沟通,协调各方的工作;5. 准备试验项目所需的文件,建立试验资料文件夹并负责试验资料的保存;6. 负责试验药物/器械等物品的接收与保管、受试者管理、原始资料管理并完成相关记录等;

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临床研究员 上海博唯生物科技有限公司 上海 0.8-1.2万/月 11-18

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

岗位职责:1)参与临床研究资料的准备;2)参与CRO的筛选、评估,及其他参加单位的筛选评估;3)参与临床研究过程全过程的质量控制,项目的进度管理及研究者的沟通协调;4)参与项目相关文件的管理,物资及药品的调配;5)参与临床研究SOP的撰写;6)完成公司交代的其他相关工作事务。任职资格:1)本科及以上学历,临床医学、流行病学、公共卫生及其他相关专业;2)语言表达和沟通协调能力良好,责任心强,具备优秀的职业道德;3) 能够承受一定的工作压力,吃苦耐劳,适应经常出差;4)熟练操作电脑,具有一定的英语听说读写能力。欢迎投放您的简历至招聘邮箱hr@bovax.com.cn,我们会尽快进行阅评,之后再决定是否与您面谈,谢谢!

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听力师 上海力声特医学科技有限公司 上海-浦东新区 0.3-1万/月 11-18

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

岗位职责: 1、 负责产品的术前、术中、术后相关临床技术支持培训工作; 2、 负责临床试验跟进和数据收集; 3、 配合销售完全技术支持工作; 4、 负责医学、销售数据的收集和录入。 任职资格: 1、 医学、护理、听力学或言语听觉、公共卫生、 医药相关专业中专及以上,有耳鼻喉科临床医学、人工耳蜗或助听器相关工作经验者优先考虑。 2、 善于沟通和应变,工作热情有责任心,能出差。

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临床监察员 上海葆年生物科技有限公司 上海-松江区 0.6-1.2万/月 11-18

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

1. 具体负责公司临床项目的计划、开展和管理、协条等;2. 协助设计、编写、制作临床试验方案和病例报告表格的设计、研究者手册与试验相关资料;3. 协助开展研究单位的调研筛选、协议谈判,召开临床试验各阶段会议,准备临床试验样品、资料及随机物品;4 负责临床试验的实施和监查工作,跟踪协调,确保研究者按照方案、GCP、SOP等相关要求进行试验,确保试验符合伦理要求、试验数据科学可靠并及时收集,确保研究中心按照时间表完成病例;5.按照检查计划定期对研究中心进行实地监查,并在规定的时间内完成监查报告,同时将访视的详细情况报告上级,使上级随时了解试验执行过程中的情况,及时发现和改正存在的问题;6.协助上级完成产品立项阶段的临床试验工作评估,与临床医院及相关临床试验员保持良好的关系;7.记录报告临床试验及不良事件与严重不良事件;8.负责临床试验相关文件的备案、归档和管理;9.能独立完成领导安排的任务。任职要求:1.本科及以上学历,3年以上临床研究工作经验,医药、临床相关专业;2.掌握GCP及临床试验法规,熟悉临床试验方案和研究流程;3.良好的沟通能力,良好的领悟能力,良好的执行能力,良好的解决问题能力。

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临床项目助理 CTA 再鼎医药(上海)有限公司 上海-浦东新区 0.5-1万/月 11-18

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

To provide administrative,technical and logistical support to ensure timely and efficient execution of clinical trials, and compliance of ICH-GCP, SOP and regulatory regulationsKey Responsibilities1) Set up, organize and maintain trial master files2) Assist project team on clinical trial relevant documentation for submission to ethics committee3) Assist project team on drug study supplies and other ancillary supplies4) Assist project manager on maintaining the study status tracking5) Assist project manager on agreement execution, payment and tracking of actual cost6) Enhance the communication and cooperation with cross-functional teams and vendors7) Arrange project/study meeting logistics8) Mentor new CTA when applicableRequirements:1) Bachelor degree or above, or equivalent, in life science area is preferred2) 1-year working experience with Clinical Research Coordinator or Clinical Trial Assistant background is preferred3) Basic knowledge in ICH-GCP, China GCP4) Computer literacy desirable5) Professional use of the English language; both written and oral6) Excellent oral and written communication skills

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研发主管 上海现代中医药股份有限公司 上海 1-1.5万/月 11-18

学历要求:|工作经验:2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:组织协调开展公司产品各个环节的研发工作,包括但不仅限于开展海外临床试验,新药注册申请等。任职资格:1.具有新药研发的专业知识,包括药学和医学的基础知识;2.熟悉国内外药物研发相关法规;3.具有信息收集、文献检索、数据整理和分析的能力;4.具有诚实、守信的品德,做事严谨、认真;5.具有良好的沟通、协调能力;6.熟练掌握英语的听说读写。有意者请发简历至:hr@sundise.com

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临床专员 上海导向医疗系统有限公司 上海 10-20万/年 11-18

学历要求:硕士|工作经验:|公司性质:合资|公司规模:50-150人

工作职责:一、(1)对内部和外部的客户提供相关医学指导,包括项目团队及其他职能部门;协助项目管理部门满足项目时间与进度。(2)负责临床试验的规划,方案制定及其他配套文件的撰写,研究者选择,对内部和外部的人员提供医学支持;对研究安全性资料进行医学审核,数据分析/解释;对质量控制的培训业务提供医学支持。(3)负责提供相关领域的医学专业知识,对临床试验和产品生命周期全过程提供医学支持。(4)对研究方案进行审查和编辑,保证信息准确,满足法规及公司内部要求。(5)撰写和审核提交给监管当局和用于学术交流的临床科学报告。(6)培养和维护与有影响力的学术领袖在医学界的关系。(7)医学文献汇编。(8)参与国内,国际和区域学术会议,收集和整理总结会议中讨论的当前医疗热点问题和发展趋势。(9)审查产品的教育,宣传和报告材料。" 二、支持医生发起的临床研究项目,协助前期文献检索,系统评价和研究设计,合同的起草和进度跟踪,关键节点的跟踪,与关键医生的沟通和协助 三、支持专业教育和培训,包括专业教育的方向性指导,学术知识分享、宣传期刊供稿、学术考核制度与教材制定等,支持市场部工作。任职资格:硕士及以上学历,医学相关专业;熟练掌握医学本专业和相邻专业知识;熟悉循证医学知识和临床研究设计及执行;有较强的组织协调、沟通谈判、团队管理能力;英语听说读写熟练。

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医学部专员 上海瀚锐医学科技有限公司 上海-杨浦区 6-8千/月 11-18

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

岗位职责1、 收集整理相关技术的文献资料2、 协助销售部、市场部医学方面的支持工作,协助相关项目的演示和讲解3、 负责公司医学技术的培训工作、远程培训工作、远程评估工作岗位要求1、医学类专业大专以上学历,3年以上相关工作经历2、熟练运用OFFICE软件,精通PPT制作者优先3、善于沟通,表达能力强,具有进取心和责任感

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临床研究协调员/CRC- 上海(五险一金,福利多) 西藏瀚科医药服务有限公司 上海 0.4-1万/月 11-18

学历要求:大专|工作经验:|公司性质:创业公司|公司规模:少于50人

1. 协助研究者完成伦理资料递交、药理机构备案及合同签署等工作;协助及时完成 SAE 及SUSAR 等相关安全报告 2. 协助研究者完成试验各个阶段研究中心的文档收集、整理、归档; 3. 协助研究者完成受试者管理工作,包括受试者招募、筛选潜在的受试者、安排受试者访视、安排实验室各项检查、获取检查结果等; 4. 协助研究者完成试验标本的处理、保存和运送工作; 5. 协助研究者完成临床研究药物及其相关物资的管理和计数,包括药物及其相关物资的接收、保存、分发、回收和归还,并完成相关记录; 6. 在研究者授权下协助研究者填写病例报告表及差异解决(需要进行医学判断的除外); 7. 协调 CRA 的中心访视工作,提前准备各种文档供 CRA 监查; 8. 按照试验计划与中心人员及申办方等进行全面的沟通(邮件、口头、传真)并记录; 9. 协助研究者完成临床试验的其他相关工作。 职位要求: 1. 临床医学、药学、护理学或相关专业,专科及以上学历,护理专业有护士执业资格证优先 2.对临床医学工作内容有一定了解,对药物临床研究感兴趣 3.良好的组织协调及多任务处理能力 4.良好的书面、语言表达及沟通能力 5.熟练使用office办公软件如word、power point、excel及outlook 6.能够快速适应新的环境及学习新知识的能力

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CLINICAL TRIAL SUPERVISOR (临床试验主管) 上海爱的发制药有限公司 上海-黄浦区 0.9-2.5万/月 11-18

学历要求:本科|工作经验:5-7年|公司性质:合资|公司规模:150-500人

Job offer: CLINICAL TRIAL SUPERVISOR We are going to recruit a Clinical Trial Supervisor for our subsidiary based in Shanghai (200 employees, 200 MRMB in Sales with aggressive and exciting plan in China); the position is based in a downtown location in Shanghai with regular trip within mainland China and occasionally in APAC and Europe.This is a company operating in the pharmaceutical industry and this locally on the entire value chain (development, formulation, production, sales);The Clinical Trial Supervisor / Clinical Search Supervisor will report to Regulatory & Medical Affairs Director 3 years local contract with 6 months probation period.Job Responsibilities: - Maintains a level of medical-scientific knowledge in an assigned therapeutic area and/or disease state(s) involving clinical issues related to relevant products- Organize and manage the clinical trial for the purpose of registration and marketing promotion.- Draft the protocol for the BE study and clinical trial.- Responsible for the project plan and budget for clinical trial.- Ensure that clinical trial compliance with the policies, protocol, schedule and SOP.- Participate in the new product launch activities as a medical expertise for explaining some medical background/ clinical results and answering related questions.- Cooperate With other departments to carry out research projects and the evaluation, particularly in the clinical part of the assessment- Organize and manage the clinical trial. Monitor the entire clinical trial process, familiar with the clinical trials from Phase I to Phase IV.- Responsible for choosing the institution, draft the agreement and negotiate for clinical trial. - Responsible for the project all kind of coordination work in the implementation process. Keep and Maintain good communication and coordination with researchers,- According to the testing requirements for the project to properly establish and manage the documentation.- Provide the clinical trial document for the drug registered.Marketing missions - Keep contact with specialists in medical field to obtain certain marketing information.- Regularly retrieve medical and marketing information for related products.Relationship Management - Active participation, communication and collaboration with R&D team, BD, Marketing and Project department.- Creative, Team player, problem settled and work under pressure- Build lasting relationships with clients and prospects- Maintain good working relationships with colleagues, senior and junior colleagues across the business unit. MANDATORY KNOWLEDGE – SKILLS AND ABILITIES- Master's degree major in medical science or pharmacy- At least 3 years relevant experience with multinational pharmaceutical company, Experience as a doctor in hospital is preferred- Fluent and professional English and Mandarin (writing and speaking)- Existing network and relationship in pharmaceutical industry- Natural commercially oriented and experienced in business development in pharmaceutical industry in China - Knowledge of China pharmaceuticals market, rules and regulations on drug development - Clinical research experience, project management experience and experience in clinical operations; or equivalent combination of education, training and experience in depth knowledge of, and skill in applying - Familiar with applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines DESIRED KNOWLEDGE – SKILLS AND ABILITIES- Depth therapeutic and protocol knowledge - Ability to set up the budget and control costs- Strong organizational and problem solving skills - Demonstrated ability to deliver results to the appropriate quality and timeline metrics - Good team leadership skills, good judgment and effective presentation skills - Establish and maintain effective working relationships with clients.- Software and computer skills, including MS Office applications

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Patient Education Specialist 山德士(中国)制药有限公司 Sandoz (China) Pharmaceutical Co., Ltd. 上海-浦东新区 1-1.5万/月 11-18

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

Job Description:1. Execute patient program action plans locally with guidance from central patient manager.2. Work with physicians/nurses to recruit patients for the patient program, gather patient info and input patient data into patient database upon collection.3. Oversee the local execution of patient club benefits / features offered to patient members.4. Organize and implement other local patient activities designed by the patient program(s). Track performances of the activities.5. Update central patient manager with patient feedback on the program.6. Collaborate with local MSLs to develop customer insights and share with PPH central team, marketing brand teams, and other functions.7. Follow the guidances of Ethic and Compliance and SOPsMinimum requirements:? Bachelor’s degree or above from renowned medical schools or traditional Chinese medicine schools.? Outstanding verbal and written communication skills in Mandarin.? Fluent in English is a strong plus.? Fresh medical school graduates acceptable; experi-ence of practicing medicine or working in pharmaceutical industry a good plus.? Good execution and organization skills.? Good interpersonal skills and caring personality.? Passion for healthcare and patient interaction.

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Clinical Project Manager 辉瑞(中国)研究开发有限公司 上海 11-18

学历要求:本科|工作经验:8-9年|公司性质:外资(欧美)|公司规模:10000人以上

The Clinical Project Manager (CPM) will lead and manage the core cross functional study team and is the single point of accountability for the operational delivery of one or more clinical studies from concept through reporting, including inspection readiness, submission and regulatory defense.The CPM is an expert on the operational delivery of clinical trials and brings that expertise to the design &; conduct of clinical studies in alignment with the program and portfolio strategies for the specific category(ies). The CPM will be responsible for developing timelines and budgets for their clinical studies and leading the execution of these studies according to time, cost and quality targets. The CPM is responsible for proactive operational risk management for their clinical study(ies). This role will be accountable for planning and delivery to the Best-in-Class targets as well as optimal resourcing of the study team(s) and ensuring optimal study team(s) health.? Accountable for managing overall study timelines, budgets and quality targets? Accountable for building, forecasting and managing the Clinical Trial Budget? Leads the core study team; manages, facilitates and documents core study team meetings (e.g. meeting agendas &; minutes, action logs and decision logs) and facilitates effective decision making? Ensures adequate study team resources (escalating to Asset team where required) and leads study team to ensure that study team structure, including sub-teams, are effective and efficient? Fosters optimal study team health including formal team effectiveness assessments and action planning? Manages study team communications to ensure cross-functional connectivity among study team members and supporting functional lines? Leads and oversees the study risk planning process (e.g. IQMP)? Oversees operational metrics across study and manages trends and escalations? Accountable for delivery to Best In Class metrics? Acts as a single, authoritative source of the study information and leads study level status reporting per organizational norms and expectations with support from Study Management for site level updates.? Ensures maintenance and accuracy of Standard Operating Procedures (SOP) log? Leads awareness and resolution of Significant Quality Events (SQEs) and escalations? Leads the study work order and change order processes? Ensures comprehensive operational input to protocol design? Monitors and remediates quality metrics and completes remediation tracker? Responsible for inspection readiness at a study level with site facing activities such as self-inspection remaining the responsibility of the Study Management group? Ensures Quality Gate timing planning, and team readiness? Responsible for obtaining requisite operational governance approvals per organizational norms and expectations. Leads preparations and presents the study to operational governance? Provides clinical timelines and costs for feasibility scenario planning to support Asset Team decision making process? Provides clinical timelines, cost, and operational risk sections of the governance presentations, memos, and other materials used for decision making. Participate and may present assigned study(ies) in part or in full to technical and executive governance.? The CPM will champion operational excellence to provide continuous improvement of processes and sharing of best practice? Partner with Project Planner and study team members to develop study level plans and processes to ensure alignment with overall Development Plan? Propose alternative study operation strategies to optimize the use of time, cost and resources.? Maintain and enhance knowledge in disease and technical areas and in global / China regulations/ guidelines pertaining to clinical trialsCPM:Skills:? Ability to lead cross-functional teams, identify, resolve &; escalate issues? Ability to represent &; communicate clearly at Governances including at the Global Level.? Ability to understand and assimilate high-level data from all functionsQualifications (Training, Education &; Prior Experience):Training and Education Preferred:? Extensive clinical trial conduct, global clinical trial operations, and a thorough understanding of the processes associated with project and study management, knowledge of Good Clinical Practices (GCPs), monitoring, clinical and regulatory operationsCPM? BS – minimum of 8 years relevant experience? MS/PhD – minimum of 5 years relevant experiencePrior Experience Preferred:? Broad experience in a Clinical Trial Execution discipline (e.g. senior study management expertise, lead data management expertise, clinical leadership expertise)? Demonstrated project management / leadership experience? Experience in understanding of key drivers impacting budgets? Experience in building a Clinical Trial Budget and managing project to budget

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Application Consultant - 临床顾问 飞利浦(中国)投资有限公司 Philips (China) Investment Co.,Ltd. 上海 11-18

学历要求:|工作经验:|公司性质:外资(欧美)|公司规模:10000人以上

Department Introduction – 部门介绍: 飞利浦医疗科技是全球最有影响力的医疗技术公司之一,通过向医疗整体解决方案转型,飞利浦医疗正借力这部新引擎成为飞利浦新的增长点,处于竞争激烈的市场前沿而保持领先优势。SCS- Solution Customer Service部门正是应时之需,应运而生,在飞利浦布局智能大健康之时,结合多年医疗设备经营的优势,向整个行业提供专业的咨询和整体方案服务。该部门聚焦的是医疗信息系统的方案设计、开发、测试和现场的实施,以及其上下游的专业咨询和支持服务。无论是IT运维、开发、集成、测试、临床顾问、技术支持或者项目管理,都有完善的职业发展路径,同时,通过精细化的培训、矩阵式的管理、高效开放的文化建设以及绩效激励机制,使得每个成员都能在相应的舞台上,获得尊重、认可和发展。 THE POSITION-- CS SCS Application Consultant – 临床顾问 该职位为飞利浦医疗科技SCS部门招聘项目临床顾问,一旦录用,将提供完善的培训和职业发展和晋升通道,并在飞利浦医疗转型中,提供实现个人和公司发展双赢的舞台Key responsibilities:- 售前和项目经理、解决方案架构师合作,对医院科室提供临床咨询服务,帮助完善客制化的解决方案并促成销售进单- 作为飞利浦信息系统和医院需求的窗口,将客户需求转化为系统需求和目标,并帮助后方工程师理解需求;- 对医疗信息系统进行临床应用配置辅助实施,并对客户进行相关培训,确保项目实施的效果和满意度;- 指导、培训其他工程师或顾问的工作,发挥各自独有领域的特长或经验,并在团队内共享成功经验;- 与客户或第三方进行有效沟通,进行多任务管理和协作,并和客户建立良好关系Key competences / experiences:- 统招高等专科以上医疗、护理、生物医学或相关专业- 2年以上临床或医院医师经验,特别是导管室,呼吸科,ICU或者影像科影像处理相关的医生或护士优先;- 对IT和信息系统有较好的基础,特别是用过医院的信息系统,如HIS、EMR、PACS系统或对医院流程熟悉者优先;- 善于沟通交流,工作细心积极主动,具有高度的责任感和较强的学习能力,可以承担较强的工作压力及强度,能适应出差,英语听说读写流利;THE POSITION-- CS SCS Application Consultant The healthcare market is moving to integrated solution space, and over the next several years, the challenge to ourselves is to be able to keep our modality engine going with improved productivity, hitting our AOP, and at the same time, we shall ignite our growth engine to get ourselves to be at the forefront of the competitive market place. In this regard, we shall free up and/or reorganize part of our resources to drive in the solution and services space. This is a very important step in operationalizing Philips’ HealthTech Strategy which will stay with us for a long time.The Application Consultant is responsible for providing professional, clinical training, education and clinical services to customers for products and solutions in Philips product portfolio. In the customer’s environment, it is essential for the CS to establish relationships with clinicians and leadership.Typically, clinician will be nurses, technicians, physicians or other allied health professionals. In addition, the CS will collaborate with project, technical and other clinical resources meet customer expectations with their Philips solution.Key responsibilities:- On time finish project task assignments.- Ensures that the clinical application implementation for project and key account.- Support CS sales pursuits as pre-sales and marketing activities needed.- Develop key account as demo site and prepare customer success story.- Share knowledge and experience within CS China.- Set up solid training to train/share with cross-region.- Support clinical related event of post service by assignment.Major Challenges:- Work professionally and effectively to deliver clinical consultant service.- Being consultant of clinical user and healthcare industry insights.- Professional in clinical domain with better than average IT competence.- Multi-tasks management and collaboration.- Demonstrated problem solving ability and Multi-tasks management.- Ability to build strong relationships with both internal and external customers.Key competences / experiences:- University degree in Nursing /Physician or equivalent in allied health discipline- Minimum 3 years’ experience in clinical environment preferably in hospital setting- Knowledge of clinical workflow within the domain of critical care or anesthesia / operating room.- Exposure or experience in delivering clinical training- Excellent customer facing and service skills is desirable.- Ability to complete tasks independently with minimal guidance.- High-level professional demeanor and interpersonal communications skills; superb writing skills in local language and English.- Deliver required results with high levels of customer satisfaction, both internal external.- Demonstrates punctuality and efficient work habits. Able to self-direct and to effectively manage priorities.- Strong organizational, time management and planning skills in order to be successful in a role performing a wide variety of tasks associated with varying customer needs, and an ability to change focus quickly as demands change.If you are interested in this position, please send your CV to Ruby Chen (ruby.chen@philips.com).

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