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遗传办专员南京希麦迪医药科技有限公司北京-朝阳区1-1.5万/月07-04

学历要求:本科|工作经验:1年|公司性质:合资|公司规模:500-1000人

岗位职责:1. 负责HGRAC的提交和审核,包括但不限于按照HGRAC规定完成网上申请表、纸质文件收集和纸质档案提交等;2. 负责在线申请结果的跟踪,定期更新HGRAC官员的拒绝原因,并与项目经理合作,制定应用策略和潜在解决方案;3. 熟悉最新的HGRAC相关法规,为项目组提供相关的遗传办问题咨询;4. 执行直线经理指派或要求的其他任务。任职资格:1. 医药学相关专业的学士(或以上)学位;2. 良好的沟通技巧和积极主动的工作态度;3. 积极主动,独立工作能力强;4. 有较强的计划和组织能力;5. 在多个职能部门环境中与多个主管/同事合作的意愿,重视团队合作的重要性;6. 有1到2年的HGRAC申报工作经验

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NGS Assay Development Scientist浙江数问生物技术有限公司杭州-拱墅区2.1-3.8万/月07-04

学历要求:博士|工作经验:3-4年|公司性质:民营公司|公司规模:50-150人

We are looking for an enthusiastic scientist to join a team dedicated to develop first/best-in-class NGS products.      Key Responsibilities:Perform proof-of-concept and hands-on experiments (wet lab)for NGS assay development activitiesApply cutting-edge technologies to realize LoD of 0.01% (mutant to wild type) in the sample of circulating cell-free DNAProvide technical advice, operating procedures, training and troubleshooting support for new technologies emerging from Assay DevelopmentManage projects in a way of PMP (Project Management Professional) and design control, reduce the delay and biasCommunicate and present work progress by written reports and oral presentationSupport other team members and their projects.Contribute to laboratory management activities.                                RequirementsEducation/Qualifications: PhD in Chemistry, Biology, Genetics or Biomedical Science, fluent in English and ChineseAt least 2 years of NGS assay development experience in a regulated environment with an established quality management system ISO13485, successfully developed a regulatory-approved NGS products is a plusAbility to work independently with minimal supervision in a team-oriented environment Excellent organisation, time management and communication skillsExcellent analytical troubleshooting skills and attention to detail Strong interpersonal skills with ability to influence and build relationships

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NGS肿瘤数据分析员上海金域医学检验所有限公司上海-浦东新区1-1.5万/月07-04

学历要求:硕士|工作经验:1年|公司性质:上市公司|公司规模:5000-10000人

1、对NGS肿瘤测序数据进行分析,撰写相关临床检测报告2、提供后续针对客户的报告解读及咨询3、对本地数据库进行维护及更新整理4、对市场、业务进行专业知识培训5、参与临床科研及文献检索,提供医学信息支持

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SAS Programmer-上海(Contract)杭州泰格医药科技股份有限公司上海1-1.5万/月07-04

学历要求:本科|工作经验:2年|公司性质:合资|公司规模:5000-10000人

工作职责:Able to conduct programming daily works independently, including generate TFLs, SDTM/ADaM mapping and specification development, QC and documentation, etc.? Write, modify, and maintain SAS programs for the creation of ADS and TFLs in an efficient manner.? Perform program validation and quality control of ADS and TFLs produced by other programmer.? Identify the programming issues and fill the issue and action tracking log where applicable.? Update the programming quality control record with programming or QC details.? Provide programming support for data management and data validation as needed.? Understand, execute and improve company SAS macros.? Produce the derived dataset specifications, programming specifications, and other process supporting documents.? Learn internal and external SOPs/WPDs, ICH-GCP and/or other international/local regulatory requirements.? Ensure all statistical activities in accordance with internal and external quality standards, SOPs/WPDs, ICH-GCP and/or other international/local regulatory requirements.? Improve technical skills including SAS programming, statistics and clinical trial through self-learning, coaching, internal training, external training, and on-job training, etc.? Develop effective team communication and team work.? Proactively participate in process/quality improvement initiatives.任职资格:At least 2 years full time work experience as SAS programmer thoroughly supporting clinical trial.? Bachelor degree or above? Familiar with CDISC. ? Nice to familiar with R, python, etc? Experience in Oncology is desirable? Have good capability in self-learning, communication and planning.? Better to have experience in global pharmaceutical company studies? Better to have strategic thinking and risk management sense.? Be capable of working under high pressure Requirement on EN ? Listening-able to take EN training and meetings? Speaking-able to communicate with EN speaking people clearly? Reading-able to read EN protocol and academic materials? Writing-able to write EN e-mails and reports

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临床数据管理员(DM leader)上海有临医药科技有限公司上海-浦东新区2-4万/月07-04

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:150-500人

工作职责:1、 协调临床数据管理过程,参与临床研究相关项目,保证临床研究数据的及时性、真实性、准确性和完整性,进行数据项目的资源、成本、质量管理的日常工作;2、 根据临床研究方案,在规定时间内完成eSource系统的设计/建立/验证/测试,以研究中心(site)为中心开展DM工作;3、 对公司内部项目相关人员(如CRA,CRC,PM等)进行eSource系统的培训;4、 为临床研究项目制订DMP,DVP,并按计划提交数据管理报告;5、 为经验较少的员工提供培训和指导;6、 负责担任数据管理相关SOP的作者或审阅者;7、 参与临床研究方案数据管理部分的撰写;8、 数据库及相关管理文件的归档;9、 完成直线经理分配的其他工作。任职资格:1、 全日制本科及以上学历(硬性条件),医药类、生物化学类等专业(软性条件,优秀者可放宽);2、 具备GCP、临床研究、临床试验流程和相关法规要求及术语的应用知识;3、 三年以上数据项目管理(肿瘤癌症项目优先考虑)相关工作经验;4、 良好的组织、沟通能力和出色的逻辑思维,善于团队合作。

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遗传分析师杭州金诺医学检验实验室有限公司杭州0.8-1.5万/月07-04

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

工作描述:1、负责二代测序基因检测结果的数据分析、报告撰写及报告解读;2、负责跟踪国际最新医学指南、规范及科研动态,并整理相关文献和完善项目数据库;3、负责业务相关的遗传咨询、医学指导及技术支持;4、完成领导的其他任务;岗位要求:1、本科及以上学历,医学、遗传学和生物医学相关专业;2、具有一年以上NGS检测结果分析工作经验者优先;3、具备优秀的文献检索与阅读能力,较好的英文读写能力;4、能够熟练使用和查询相关数据库;5、具有较强的自我学习能力和责任心,有良好的团队协作精神;

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初级遗传基因师慧算医疗科技(上海)有限公司上海-浦东新区1-2万/月07-04

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

1、负责审核基因检测报告;   2、负责基因检测报告解读,相关基因文献整理,协助客户理解基因检测结果;   3、负责根据客户需求,制定相应基因检测方案;   4、负责为客户提供技术支持,以及技术相关讲座;   5、负责对公司内部人员进行技术知识培训;   6、完成领导交办的其他任务。     任职要求:   1、本科或硕士,医学、遗传学、生物学、生物信息学等相关专业;   2、熟悉遗传学基本原理,了解基因检测、遗传疾病以及分子生物学相关知识;   3、有良好的英文文献阅读和综述能力;   4、具备高度责任心、良好的沟通能力以及团队协作能力。        

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数据管理员北京慧智康健医药科技有限公司北京-石景山区4.5-5千/月07-04

学历要求:本科|工作经验:无需经验|公司性质:民营公司|公司规模:少于50人

岗位职责:- 负责临床研究数据管理部分的整体工作,包括跨部门沟通、参与项目启动工作- 撰写数据管理计划- 使用EDC系统,进行数据库的创建、测试、上线和维护- 根据临床方案,设计CRF- 撰写数据核查计划- 进行数据核查、质疑、清理与质控- 外部数据一致性检验- SAE一致性检验- 管理数据管理过程产生相关技术文档- 撰写数据管理报告- 参与制定和维护数据管理部门SOPs- 辅助完成公司交代的其他的任务任职要求:- 医学,临床医学,公共卫生,流行病等本科以上学历- 熟悉临床研究的数据管理程序和流程- 有一定EDC操作系统操作经验- 能独立CRF设计- 熟悉ICH-GCP、临床研究相关的法律法规- 有较好的英语水平,英语四级或以上- 工作认真细致有耐心,责任心强- 良好地沟通和团队协作能力

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Clinical Data Management劲方医药科技(上海)有限公司上海-浦东新区2.5-3万/月07-04

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:50-150人

Clinical Data Management,Senior Manager/Associate Director Clinical Data Management conducts data management activities in support of Genfleet Therapeutics studies across all stages of clinical drug development. The incumbent ensures that clinical data capture, systems, and processes represent accurate, consistent, high-quality, and complete data. Additionally, the incumbent impacts multiple clinical development programs, health authority submissions, presentations, and publications across internal and external stakeholders. Responsibilities 1.     Provides clinical data management oversight of outsourced clinical trials for phase I-III studies including: project management, vendor management, coordination of internal reviews, and approval of deliverables. 2.     Act as liaison with CROs, third party data vendors, and EDC vendors. 3.     Collaborates with internal clinical study team to ensure all stakeholders’ needs are addressed. 4.     Assist as author/reviewer for CRFs/eCRFs, CCGs/eCCGs, and Data Management Plans, as well as mentoring junior staff in these activities. 5.     Oversees database design and production, ensuring that CROs, vendors and internal staff meet the highest quality standards. 6.     Oversees report specification development including patient profiles and other reports, listings and metrics supporting clinical development decisions, periodic regulatory filings and study oversight. 7.     Accountable for external data vendor documentation, management, and reconciliation. 8.     Oversight, management and mentoring responsibilities for both permanent and contracted staff in clinical data management. 9.     Contributes to the strategic oversite of clinical programs and individual Genfleet sponsored trials. 10.  Contributes to departmental process improvement, standards and integration of technology. Qualifications 1.     Bachelor’s Degree or above required. 2.     5+ years of clinical data management experience in the pharmaceutical industry, with increasing responsibility. 3.     Demonstrated proficiency managing the lifecycle of clinical data projects. 4.     Knowledge of and experience with EDC databases (especially Medidata RAVE), CDASH/SDTM standards, medical terminology, medical coding dictionaries, and quality control processes. 5.     Familiarity with GCP, ICH, CDE and FDA requirements as applicable for Clinical Data Management. 6.     Experience with drug development in oncology required.

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SAS经理/高级专员上海临领医药科技有限公司上海-静安区1.5-4万/月07-04

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:150-500人

岗位职责:1. 编写SAS程序建立ADS;2. 编写SAS程序建立统计数据清单、统计表格,生成统计报告;3. 与医学总监、CRA、数据管理员等相关项目责任人沟通,提供支持;4. 为数据管理员提供编程支持,编程核查数据;5. 对公司外包项目进行编程QC;6. 理解项目方案、SAP,必要时给出恰当建议;7. 完成部门的其他相关工作。任职要求:1. 医药、卫生统计、临床相关专业,本科及以上学历,2. 2年以上SAS经验。具医院临床科室、制药企业或CRO公司SAS Programmer工作经验者优先考虑。3. 了解ICH-GCP,了解药物研发的全过程,熟悉临床试验全过程;4. 较好的执行力和团队合作精神.

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数据分析师中国医药工业信息中心上海-静安区0.7-1.4万/月07-04

学历要求:本科|工作经验:1年|公司性质:国企|公司规模:50-150人

岗位职责: 1.参与公司数据管理工作,保证数据的及时性、准确性和一致性,积极协同产品部、开发部等部门共同优化公司数据服务 2.参与公司产品战略规划,发挥个人数据业务优势,为数据标准化方案制定、数据结构化提供支持 3.参与公司产品运作逻辑优化,设计并执行提升数据及时性、一致性和准确性的流程和方法 4. 分析数据库价值和逻辑关系,对产品部使用数据库提出建设性建议 5. 分析数据库结构和逻辑关系,对接开发部实现数据库的应用任职要求1.药学、生物、统计、计算机等本科及以上学历2.医药数据分析、数据模型搭建有经验者优先3.熟练掌握Excel中高阶技能,具有数据库(SQLServer、MySQL等)使用经验者优先4.熟悉编程语言或者数据统计工具(Python、R等)并有相关应用经验者优先 5.熟悉数据清洗、数据分析(可视化)工具者优先(Kettle、PowerBI等)

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数据分析师洁深源(武汉)节能环保科技有限公司武汉-武昌区8-10万/年07-04

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

1. 抽象数据分析需求,形成有竞争力的数据产品,帮助产品业务更深刻的理解并运用数据; 2. 基于对互联网产品和业务的深入理解的基础上,独立承担复杂分析任务,为产品方向提供决策支持;3. 负责相关项目性工作的数据支持、业务报表的制作;4. 建立产品业务相关的数据统计模型;5. 建立各个环节工作预警及时,对相关数据异常情况提前预警。任职要求:1. 本科及以上学历,计算机、统计学、数学、信息管理、社会学等相关专业, 3 年以上咨询、互联网行业工作经验;2. 良好的数据分析能力,有丰富的数据分析、挖掘、清洗和建模的经验;3. 熟悉互联网数据采集,具备大数据处理能力 , 熟练运用 SQL ,掌握 hive 等相关数据工具;4. 善于沟通,具有良好的团队合作精神;

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统计分析部-临床数据分析专员上海巧捷生物科技有限公司上海-静安区1-1.6万/月07-04

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

职位介绍-整理医学数据,制定分析思路,并进行常规数据统计分析(主要包含差异分析、关联分析、回归分析、生存分析等)。-根据统计分析结果,规范化制作撰稿所需使用的图片、表格及其它支持材料。-设计常规临床研究流程,撰写对应的研究方法(中文和英文)。-对论著编辑部及医学部提供支持。 职位要求1.专业要求-临床医学、基础医学、药学、公共卫生与预防医学、流行病与卫生统计学、环境和职业公共卫生、生物统计学等专业优先。2.经验要求-有临床数据分析、临床试验监查工作、临床数据管理以及统计分析报告撰写经验者优先。-有医学论文撰写和发表经验者优先。3.学历要求-本科及以上学历,硕士优先。4.技能要求-熟练使用SPSS统计软件、GraphPad Prism作图软件以及熟练使用OFFICE办公软件(EXCEL、WORD、PPT)。-英文水平CET6或以上(医学英语能力强者优先)。 薪资待遇-月度薪资10k-16k。-年终奖金根据业务排名另行评定发放。 公司福利-丰厚薪资待遇(每年1-2次调薪,优于行业平均水准)    -五险一金    -职业培训    -跨部门轮岗(培养综合能力)    -年度旅游(团建+年会/国内/国外旅游)    -带薪年假(10+N)    -春节返乡交通补贴    -每月交通补贴    -安家补贴    -节日礼物    -上海落户协助    -补充商业医疗保险

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Clinical Data Management强生(中国)投资有限公司上海-徐汇区20-40万/年07-04

学历要求:本科|工作经验:5-7年|公司性质:外资(欧美)|公司规模:10000人以上

Position Summary:? Type of Role: This is a professional individual contributor role that provides oversight and accountability for more than one low to moderate complexity trial or one high complexity trial. May be a member of more than one project of low to moderate complexity or member of one project of high complexity.? Impact of Decision-Making: This position makes recommendations and influences decisions for specific trials or assignments. The Senior GDM influences processes, timing, and structure for specific trials or assignments.? Accountability/Decision-Making: This position analyzes, provides recommendations, and makes decisions with direction from manager or DML.? Knowledge: This position requires In-depth knowledge of the protocol. In-depth knowledge of current clinical drug development processes is needed. In-depth knowledge of applicable international guidelines regarding data management of clinical trials is required. This position needs to understand relevant system/technical knowledge. In-depth knowledge of current industry standards (i.e., CDISC, SDTM, CDASH, etc.) is required. Knowledge of technology platforms, confidentiality for data exchange, and project management and techniques is required.? Supervision Received: Work is received in broad terms. Work is reviewed during major deliverables. Amount of instruction is limited. Work is reviewed with the Data Manager Leaders as well as with the immediate manager.? Supervision Given: There are no direct reports for this position. This position collaborates with Vendors/CROs to achieve successful, cooperative partnerships. This position may delegate tasks and assignments to Global Data Managers. The Senior GDM recognizes opportunities and contributes to solutions to strengthen the vendor/CRO relationship.? GDO Common Competencies: Primarily at the Learning or Applying Level, see Appendix for competencies and proficiency levels.? DM Specific Competencies: Primarily at the Learning or Applying Level, see Appendix for competencies and proficiency levels.Principal Responsibilities:? Takes a leadership role with the CRO, the trial customer(s) and other internal and external partners to establish, align and confirm data management expectations for assigned trial(s).? With the trial customer, CRO and other functional partners:o Gathers content and integration requirements for eCRF and other data collection tools.o Establishes conventions and quality expectations for clinical data.o Establishes expectations for dataset content and structure.o Set timelines and follow-up regularly to ensure delivery of all Data Management milestones.Version 2.0 dated 28FEB2021 (FINAL)Job ID: 10001417, Job Code: Specialist 3, Clinical Data, JOB SUBFUNCTION: Clinical Data Management(PG25), Org chart title: GLOBAL DATA MANAGERPage 2 of 4For Internal Use Only? Performs trial level oversight controls as described in the oversight plan, QC process and work instructions with minimal DML direction.? Reviews clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format and consistency. Ensures compliance with regulatory guidelines and the documentation matrix.? Ensures real-time inspection readiness of all DM deliverables for the trial; Participate in Regulatory Agency and J&J internal audits as necessary.? Plans and tracks content, format, quality, and timing of data management deliverables, including, but not limited to, CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival. Ensures deliverables are on time.? Takes a leadership role with the assigned clinical working group(s) to ensure that DM and TA trial needs and deliverables are met.? Identifies and communicates lessons learned, best practices and frequently asked questions at the trial level.? Identifies and participates in process, system, and tool improvement initiatives within DM.? Presents and trains at investigator and monitor meetings.? May undertake the principal responsibilities of a CDM, as appropriate.

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临床数据管理员 Data Managment昆翎医药厦门1-1.5万/月07-04

学历要求:本科|工作经验:3-4年|公司性质:合资|公司规模:1000-5000人

工作职责1、负责并参与完成临床试验的数据管理工作;2、参与项目启动工作,编写数据管理计划;3、编写数据核查计划及程序;4、撰写数据管理报告;5、负责项目的整体进度跟踪管理;6、解决数据管理过程中出现的问题。任职资格1、医学,药学,医学信息管理,生物,公共卫生,自然科学,医学统计,或相关专业本科或以上学历;2、3年及以上临床数据管理经验,使用过SAS、SPSS、EXCEL等统计分析工具,有编程和数据库方面知识和经验;3、工作认真细致有耐心,责任心强;4、良好地沟通和团队协作能力有较好的英语水平,英语四级或以上;5、良好地组织和计划能力,能够合理安排在多项目多重时限下的工作优先次序,以按要求期限完成工作;6、具有较强的学习能力,乐于持续地学习,能尽快掌握具体工作中所需专业知识和技能,并主动提高自己的业务水平。

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应用工程师成都好映像科技有限公司成都3-8千/月07-04

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、负责公司销售产品项目的技术支持、协调及临床应用。 2、负责与客户沟通,随时更新客户要求信息,并向客户汇报项目状况; 3、负责向客户提供先期解决方案和建议; 4、协助项目经理进行供应商评定或推荐; 5、现场支持系统总装、评估及应用,负责解决系统级工程问题。 任职资格: 1、医学检验等相关专业大学专科以上学历; 2、具有技术交底、应用指导、调试测试等所有技术工作能力

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初级遗传解读师赛福基因苏州5-7千/月07-04

学历要求:本科|工作经验:1年|公司性质:民营公司|公司规模:150-500人

1、样本信息及病例整理;2、协助完成临床基因检测报告撰写;3、遗传病数据解读相关医学知识库的整理收集,修订和更新。   任职资格:1、学历:本科及以上学历;2、专业:医学,生物学等相关专业;3、专业知识:有医学文献阅读转化能力;4、工作经验:优秀应届毕业生即可;5、素质要求: 工作积极主动,严谨仔细,诚实可靠,责任心强。

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数据分析员花安堂生物科技集团有限公司广州-番禺区4.5-6千/月07-04

学历要求:本科|工作经验:1年|公司性质:民营公司|公司规模:150-500人

技能要求:数据库构建,生物统计学,数据建模,数据挖掘,统计分析,数据分析岗位职责1.全面掌握最新临床疗效评价与感官评价相关数理分析方法;2.选择精准的临床数据处理方式;3.能有效地把关方法及时间数据的统计;4.负责数据库的维护管理工作。岗位要求:1.本科及以上学历,数学、统计学、物理学、医学等相关专业,对统计分析工作感兴趣;2.有相关化学、生物相关检测、评价经验,或会使用功效评价相关仪器者优先; 3.有基本的自主发现问题、思考问题和解决问题的能力;4.善于沟通、性格开朗、认真踏实、有合作精神。

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湛江久和医院--数据分析员深圳爱维艾夫医院管理有限公司湛江4-5千/月07-04

学历要求:大专|工作经验:1年|公司性质:民营公司|公司规模:150-500人

湛江久和医院--数据分析员岗位要求:1.大学专科及以上学历,数学、统计、计算机等相关专业毕业,1年以上数据分析相关工作经验,优秀的应届毕业生也可考虑,有数据分析师证书***。2.熟悉SQL查询,熟练使用 EXCEL、PPT等工具,能独立撰写数据分析报告,***能熟练操作python、Power BI等工作。3.具备一定的分析和解决问题的能力,逻辑思维能力和数据敏感性较强。4.工作上能做到积极主动,认真严谨,并且可以胜任重复性的工作,能接受挑战和承担一定的压力。5.具有良好的团队沟通和协调能力。    医院提供五险一金、团体意外险,旅游、年终奖、节日福利等,每天工作7.5小时,每周工作5.5天,享受法定假、年休假等福利待遇。有意者请发简历到邮箱542506400@qq.com   联系电话:杨小姐3303880

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EG-Safety Data Management Specialist(J15855)辉瑞(中国)研究开发有限公司武汉6-8千/月07-04

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

工作职责:Position PurposeReview, preparation, and completion of reports of adverse drug experiences, to determine the safety profile of Pfizer’s products and to meet regulatory requirements. Determination of local submission of individual and, where appropriate, aggregate safety reportsPrimary Responsibilities Carry out case processing activitiesReview, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency.  Process cases based on these assessmentsReview case criteria to determine appropriate workflow for case processingAssess cases to distinguish those with particular complexities and/or specific issues, and escalate appropriatelyWrite and edit case narrativeDetermine and perform appropriate case follow-up, including generation of follow-up requestsReview processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenariosLiaise with key partners, locally , and other stakeholders regarding safety data collection and data reconciliationDevelop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety databaseDetermine reportability of scheduled reports , ensuring adherence to regulatory requirementsConsistently apply regulatory requirements and Pfizer policiesParticipate, as appropriate, in local, internal and external safety activities任职资格:Technical Skill RequirementsExperience in pharmacovigilance and/or data management preferred but not requiredExperience and skill with medical writing an advantageDemonstrated computer literacyExperience in use and management of relational databases preferredQualifications (i.e., preferred education, experience, attributes)Health Care Professional or equivalent experience preferredAbility, with supervision, to solve routine problems and to surface issues constructivelyAbility to make basic decisions with an understanding of the consequencesAbility to achieve personal objectives while meeting departmental standards of performanceAbility to work under supervision in a matrix organizationFluency in spoken and written English

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