您所在的位置:最新招聘信息 >全国职位信息 >沈阳招聘网 >沈阳临床数据分析员招聘信息

职位推荐:物理教师/老师电子生产储备干部装修顾问flash动画实习生陈列师餐饮储备店长金融销售精英风控总监房产经纪服装买手临床推广经理网络维护总账会计VP3D动漫设计

职位分类:不限

更多
更多:

已选条件:
沈阳临床数据分析员
清除条件
全选
申请职位

临床数据管理经理大连展锋文化传媒有限公司沈阳2-3万/月06-24

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

岗位要求: 1)医药相关专业本科以上学历; 2)3年以上临床数据管理(clinical data management CDM)经验优先,英语具备读写能力; 3)有项目管理或团队管理经验优先。如果没有管理经验,未来可以朝管理方向培养。   职位描述: 独立完成临床试验中整个数据管理的相关工作。为医学、临床操作和统计团队提供数据管理方面的支持。撰写数据管理相关文件,例如数据管理计划、病例报告、数据结构说明书、数据核查计划、电子病例报告填写指南和数据管理报告等。执行EDC系统的用户接受测试。确保在EDC系统中的临床数据被高质量地进行锁库/解锁和冻结/解冻以满足统计审阅、内部审阅和最终锁库等需要。执行严重不良事件一致性核查和实验室数据核查。使用MedDRA和/或WHODrug进行医学编码。管理和培养初级数据管理员。参与DM的SOP和体系的建设。参与其他相关工作   任职资格: 1. 医药相关专业本科以上学历,医药学类专业为佳,数学,统计,计算机,英语均可 2. 有3年以及以上的临床数据管理工作经验 3. 英语4级,读写熟练,英语6级优先 4.良好的沟通技巧和团队合作精神 5.深刻理解临床试验药物开发流程、临床试验数据管理的行业标准和相关的CFDA/FDA法规、指导原则 熟悉Office软件。   联系方式如下: 联系人:Kitty Yang 手机号: 13478553381 电话:0411-39707283 电子邮箱:Kitty@china-genius.com  

立即申请
收藏

Associate Programmer AnalystPPD沈阳-沈河区0.8-1万/月06-24

学历要求:本科|工作经验:1年|公司性质:外资(欧美)|公司规模:150-500人

PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. We are passionate about being data and technically agile and driving enhanced value for our clients and patients. Determined to improve patient health, we help PPD provide industry-leading statistical, programming and clinical pharmacology contributions through global delivery, consistent quality adherence and scientific insight. As an Associate Programmer Analyst you will perform programming support tasks as assigned by study project team leads. At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. Summarized Purpose: Provides bioinformatics programming support for some or all of the following activities: creation and maintenance of programs used for data management, data validation, analysis data, statistical report generation, and program validation. Communicates effectively within a multi-disciplinary project team to complete assigned tasks on time and within budget. Essential Functions:??? Performs programming support tasks as assigned by study project team leads that includes but is not limited to creating, executing, maintaining, and validating programs that transfer data across multiple data management systems or operating systems, combining data from a variety of sources and structures, generating and storing summary data from a variety of sources, generating reports or combining multiple databases and validating programs that generate listings, tables and figures using SAS and standard tools and processes. Actively seeks information to gain a good understanding of the programming role and the overall process, including following departmental working practice documents and SOPs. Documents all work and manages own assignments to meet timelines and deliver high quality. Functions as a team member by working with study team leads to ensure they are kept informed of progress on tasks assigned. Increases knowledge base and professional skills in areas including programming, technology and techniques, clinical trials, and the pharmaceutical industry by working closely with mentors, attending presentations / teaching events, and contributing to other general department documents and policies by assisting mentors with implementing best practice documents and articles. Education and Experience: Bachelor’s degree in computer science, statistics, biostatistics, mathematics or related field or equivalent and relevant formal academic / vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years). In some?cases?an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.? Knowledge, Skills and Abilities: Fundamental understanding of one or more programming languages Essential attention to detail Decent problem-solving skills Decent written and verbal communications skills Basic organizational skills with the ability to adapt and adjust to changing priorities Positive attitude and the ability to work well with others Demonstrated initiative and motivation Working Environment: PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary for typical working hours. Ability to use and learn standard office equipment and technology with proficiency. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. May require travel. (Recruiter will provide more details.) PPD Defining Principles: We have a strong will to win - We earn our customer’s trust - We are gamechangers - We do the right thing - We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, then please submit your application – we’d love to hear from you

立即申请
收藏

临床数据管理 DM辽宁辉泰医药科技有限公司沈阳6-8千/月06-10

学历要求:本科|工作经验:1年|公司性质:民营公司|公司规模:50-150人

1.熟悉数据管理整体流程;2.可以进行CRF设计;3.执行数据库测试和用户接受测试;4.撰写数据管理相关文件,包括数据管理计划、数据核查计划、数据管理报告等;5.负责数据的核查与清理,第三方数据一致性核查与SAE一致性核查;6.清楚数据库的锁库等相关工作。岗位要求:1.本科及以上学历,医学或药学等相关专业;2.具有良好的沟通能力和表达能力,团队合作精神;3.1年以上临床数据管理经验,具有CRO经验者优先

立即申请
收藏

医学信息沟通专员辽宁康惠生物科技有限公司沈阳-大东区6-8千/月06-12

学历要求:硕士|工作经验:无需经验|公司性质:民营公司|公司规模:50-150人

岗位职责:  了解宏基因组病原微生物基因检测产品原理和策略,参与及推进病原宏基因组检测产品的研发与优化;负责临床医学专家关系的建立、发展和维护,实现市场营销目标,并协助完成后续科研问题的沟通和协调;开展有关成果调研、文献查询、专利检索等工作;参与公司科研及学术文献的撰写和发表;向区域市场和销售人员及时传递产品相关的最新医学信息并解答产品相关问题;定期参加行业内各项学术论坛和专家峰会,培养与行业内相关专家的良好合作关系;对于公司开展项目合作的医院进行相关产品方案的培训和交流。上级领导交代的其他相关工作。              任职资格:医学或生物学相关专业、硕士及以上学历,有医药或基因市场工作经验者有限;具有一定的英语读写能力,具有医学、生物技术和高通量测序等相关的知识;有良好的沟通及表达能力;具有饱满的工作热情和坚忍不拔的工作意志。可接受出差。

立即申请
收藏

医学专员沈阳新地药业有限公司沈阳0.4-1万/月05-29

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、 负责搜集和整理疾病领域信息、诊疗规范、临床循证等数据,追踪分析国内外研究进展,为制定医学策略提供支持;2、 负责科学准确解答不同用户诊疗、用药医学咨询,收集分析用户医学需求和面临的问题;3、 负责上市后产品临床数据的收集、管理;4、 负责组织专业知识培训,并定期进行医学新进展知识学习;岗位要求:1、 全日制统招本科及以上学历,临床药学专业,3年以上临床药学工作经验;2、 具有熟练的中英文文献检索、解读、分析、整理能力,对疾病领域进展具有持续追踪和收集信息的意识; 3、 有良好的计算机应用基础,能熟练使用Office等办公软件。

立即申请
收藏

临床数据协调员-沈阳(Contract)杭州泰格医药科技股份有限公司沈阳0.8-1万/月05-20

学历要求:本科|工作经验:3-4年|公司性质:合资|公司规模:5000-10000人

工作职责:岗位描述:执行数据管理工作1.为临床试验项目提供数据管理方面的专业支持;2.参与临床研究方案设计,制定数据管理解决方案和进度计划;3.撰写和审阅数据管理的相关文件DMP/DVP等,负责及时更新和存档;4.管理CRO DM工作质量,确保供应商提供的服务和标准符合项目要求和相关法律规定;5.审核/批准CRF/EDC的设计;6.跟踪CRF表数据和外部电子化数据的写入情况;7.参与数据库的数据审核,参与数据审核会议;8.审阅研究数据集,供临床统计分析;注:这份工作描述并没有列出所有的工作职责。员工可能会被上级或管理层要求执行其他任职资格:1.教育要求:医学、药学、护理学、数学、生物统计等相关专业本科及以上学历。2.工作经验要求:2年以上临床试验数据管理经验。3.岗位技能要求:熟悉FDA、EMA以及CFDA的数据管理相关的各项法规及指导原则,熟悉ICH指导原则,扎实的数据管理基础知识,熟悉数据管理的过程,熟悉CDISC标准。—有医学编码经验或数据库建库经验优先考虑。

立即申请
收藏

医学专员恒瑞医药-江苏科信医药销售有限公司沈阳0.8-1.5万/月05-10

学历要求:硕士|工作经验:1年|公司性质:上市公司|公司规模:10000人以上

岗位职责:1、负责搜集和整理疾病领域信息、诊疗规范、临床循证等数据,追踪分析国内外研究进展,为制定医学策略提供支持;2、负责科学准确解答不同用户诊疗、用药医学咨询,收集分析用户医学需求和面临的问题;3、 负责上市后产品临床数据的收集、管理;4、 负责组织专业知识培训,并定期进行医学新进展知识学习;岗位要求:1、全日制统招本科及以上学历,医学相关专业(临床医学优先),经验不限;2、 具有熟练的中英文文献检索、解读、分析、整理能力,对疾病领域进展具有持续追踪和收集信息的意识3、有良好的计算机应用基础,能熟练使用Office等办公软件;

立即申请
收藏

数据管理员(010985)江苏先声药物研究有限公司北京-东城区9-20万/年06-13

学历要求:本科|工作经验:在校生/应届生|公司性质:外资(欧美)|公司规模:150-500人

岗位职责:1、使用试验中的文件包括方案、病例报告表、数据清理指南等2、根据相关的指南负责撰写和关闭临床数据质疑表或应用自动更正表格3、开展用户验收测试4、开展数据核查工作5、识别和报告试验方案违背6、根据指南和受试者基本资料,撰写临床数据质疑表7、在电子数据采集系统的平台上操作锁页 8、支持临床监察员去发现找回遗留数据9、负责早期和末期的数据质量核查工作10、在项目进行中更新相关的进度系统11、定期汇报工作的进度给直接主管; 任职资格:1、医学或者药学专业本科或者本科以上2、有临床试验相关实习经验者优先。3、理科逻辑性佳;4、2021年全日制大学毕业生,本科及以上学历,药学等相关专业;

立即申请
收藏

Statistical Programmer (SAS)精鼎医药研究开发(上海)有限公司沈阳-和平区10-15万/年06-22

学历要求:本科|工作经验:1年|公司性质:外资(欧美)|公司规模:10000人以上

精鼎沈阳办招聘各个level的Statistical Programmer/SAS Programmer(1,2,Sr.),SAS经验优先。JD:Deliver best value and high quality service.Ensure quality control (QC) on all process and technical activities related to:- trial set-up and maintenance, and/or derived dataset, table, listing, and figure programming and/or implementation of system applications and upgrades/changes to those applications as required in accordance with corporate quality standards, WSOPs / Guidelines, ICH-GCP and/or other international regulatory requirements are performed.-Check own work in an ongoing way to ensure first-time quality.-Maintain all supporting documentation for studies in accordance with WSOPs/Guidelines to ensure traceability and regulatory compliance.-Proactively participate in quality improvement initiatives.-Ensure compliance with WSOPs/Guidelines, ICH-GCP and any other applicable local and international regulations and participate in internal/external audits and regulatory inspections as required.-Develop wider knowledge of areas of Clinical Data Management Systems (CDMS), Electronic Data Capture (EDC), Clinical Trial -Management System (CTMS), Safety Reporting, SAS and other programming language usage and processes within the GRO, biostatistics, and medical arenas.-Provide relevant training and mentorship to staff and project teams as appropriate.-Assist project teams in the resolution of problems encountered in the conduct of their daily work.-Assist in the coordination of project start-up activities, including Unix/PMED project area set-up, creation of global programs (e.g., setup.sas, formats.sas, etc.), tracking spreadsheets, and required documentation.-Assist in the production and QC of derived dataset specifications, programming specifications, and other process supporting documents.-Use efficient programming techniques to produce and/or QC low-medium complexity derived datasets, tables, figures and data listings.Experience:First degree (undergraduate or equivalent) in a relevant discipline is preferred or equivalent work experience.Excellent written and oral communication skills.Relevant Clinical Trial industry experienceExperience working with systems used within the Clinical Trial process (e.g., SAS, CDMS, EDC (Inform, RAVE, DataLabs), CTMS, Medical Safety Reporting)

立即申请
收藏

全选
申请职位
  • 上一页
  • 1
  • 下一页
共1页,到第确定

精英竞拍汇-中高端人才求职平台

互联网专场
招聘职位: 后端开发,前端开发,移动端开发,测试,产品/设计/运营
金融专场
招聘职位: 财务审计,合规与风险控制,后台运营,投行,销售
房地产专场
招聘职位: 房地产开发,建筑工程,规划设计,商业,市场营销
汽车专场
招聘职位: 汽车新能源,软件与汽车电子,生产制造,质量管理,供应链管理

相似职位

全选
一键申请
全选
一键申请