icf

中国icf职位233个。每日更新。

  • Behavioral Health Coach Premium

    9小时前


    China Intellect 远程 全职

    DescriptionYou will be a practitioner on our telehealth platform 'Intellect', where your role is to support our clients' mental health and personal growth based on the individual needs and goals. This is delivered primarily through scheduled 30-minute video sessions on our platform.This is a freelance remote role with the flexibility to decide your business...

  • CRA (Level II) FSP Premium

    4天前


    Beijing, 中国 Thermo Fisher Scientific 全职

    Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionSummary of Essential Functions:Prepares, reviews and coordinates, under guidance, local regulatory submissions (MoH, EC, additional special national local applications if applicable, e.g. gene therapy approvals, viral safety dossiers, import license) in alignment with global...

  • CRAII/ SCRA Premium

    1天前


    Zhengzhou, Guangxi, 中国 上海诺为电子科技有限公司 全职 ¥18,000 - ¥25,000 临时

    该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

  • CRAII/ SCRA Premium

    1天前


    Beijing, Beijing, 中国 上海诺为电子科技有限公司 全职 ¥18,000 - ¥25,000 临时

    该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

  • CRAII/ SCRA Premium

    2天前


    Harbin, Heilongjiang, 中国 上海诺为电子科技有限公司 全职 ¥18,000 - ¥25,000 临时

    该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

  • Clinical Trial Assistant Premium

    9小时前


    Chengdu, 中国 Parexel 全职

    When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

  • Site Activation Specialist Premium

    2天前


    Shanghai, Shanghai, 中国 IQVIA 全职

    Essential Functions • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project...

  • Biomarker Group Leader Premium

    9小时前


    Shanghai, 中国 Roche 全职

    At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

  • Sr. Site Activation Specialist Premium

    9小时前


    Shanghai, 中国 IQVIA 全职

    Essential Functions• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project...

  • SCRA Premium

    4天前


    Beijing, Beijing, 中国 上海诺为电子科技有限公司 全职 ¥22,000 - ¥26,000 临时

    该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

  • CRAI/ CRAII/ SCRA Premium

    4天前


    Weinan City, Shaanxi, 中国 上海诺为电子科技有限公司 全职 ¥10,000 - ¥22,000 临时

    该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

  • CRAI/ CRAII/ SCRA Premium

    4天前


    贺费, Yunnan, 中国 上海诺为电子科技有限公司 全职 ¥10,000 - ¥22,000 临时

    该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

  • CRAI/ CRAII/ SCRA Premium

    4天前


    Xin'an, Henan, 中国 上海诺为电子科技有限公司 全职 ¥10,000 - ¥22,000 临时

    该职位来源于猎聘 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

  • HGR Specialist Premium

    9小时前


    Shanghai, 中国 IQVIA 全职

    Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements  at the regional, or country level.Prepares and manages site documentation; reviews and negotiates site  documents and contracts with sites and sponsors;...

  • Site Activation Specialist Premium

    9小时前


    Beijing, 中国 IQVIA 全职

    Essential Functions• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project...

  • 医学写作高级经理 Premium

    9小时前


    上海市, 中国 研发系统 全职

    工作职责岗位职责 一、医学及注册文件撰写 负责FDA及全球注册相关医学文件的撰写、审核、质量控制及项目管理,包括但不限于: 临床试验方案(Protocol)、临床研究报告(CSR) 、研究者手册(IB) 、临床开发计划(CDP) 、知情同意书(ICF) 、IND/NDA/BLA申报资料...


  • Beijing, 中国 Novotech 全职

    Description Clinical Research Associate (CRA) Job Description The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP), and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities Job...

  • 医学经理/高级经理 Premium

    1天前


    Shanghai, Shanghai, 中国 苏州宜联生物医药有限公司 全职 ¥25,000 - ¥45,000 临时

    该职位来源于猎聘 岗位职责: 1、为公司的产品开发过程中临床研究提供支持及指导:如适应症的选择、临床研究方案设计、临床研究所需文件、资料的撰写。...


  • Shenyang City, Liaoning, 中国 康诺亚生物医药科技(成都)有限公司 全职 ¥30,000 - ¥50,000 临时

    该职位来源于猎聘 职责描述: 1....

  • Sr/Site Activation Coordinator Premium

    9小时前


    Dalian, 中国 IQVIA 全职

    Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential Functions• Under general supervision, serve as Single Point...