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该职位来源于猎聘 Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government,...

该职位来源于猎聘 Reporting To Pharmacovigilance Manager Position description: Responsible for carrying out the PV related work according to ICH-GCP, SOPs, project specific procedures, and applicable regulatory requirements. Responsibilities:  Support to set up the related system and safety database  Support the PV related work in the clinical...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part of our...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...

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...

该职位来源于猎聘 Primary Responsibilities:  Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work, SOPs (and / or the Sponsor’s SOPs as appropriate) and the ICH GCP and associated regulations. May perform co-monitoring visits and other types of site visits as needed. ...

该职位来源于猎聘 职责描述： 1. 生产现场监督：对本公司原液生产过程进行监控，包括细胞库建库、原液生产（细胞培养和纯化）过程的关键操作环节进行监控；执行关键生产过程的动态环境监测。 2.对批记录/相关辅助记录进行符合性审核。完成电子数据审核。 3....

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...

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...

Senior CRA China, office basedICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and...

该职位来源于猎聘 岗位职责 1. 作为 DMPK 领域的专家，在多学科团队中主导 PK 小组的工作，负责从早期药物发现、先导化合物优化到临床前开发全过程的 PK 研究策略制定与执行。 2. 设计、实施并科学解读创新性的 ADME 与 PK/PD...

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout...

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout...

该职位来源于猎聘 Position description: Responsible for the overall management of projects to ensure the adherence of the project to quality standards and the approved timeline and budget in the service agreements. Leads the project team and the internal/external communications and identifies suitable resources to facilitate efficiency improvement for...

该职位来源于猎聘 岗位职责： 1.负责医学文件的撰写、审阅、修订与更新，包括但不限于临床试验方案、临床试验报告、研究者手册、知情同意书、M2.5与M2.7 2.协助医学信息、医学策略、商务竞标工作 3.协助AI撰写工具的开发及完善...

该职位来源于猎聘 岗位职责： 1.负责（协助）撰写临床试验相关文档，包括但不限于：临床试验方案及修订案，研究者手册，临床研究报告，知情同意书等；...

该职位来源于猎聘 【岗位职责】： 1、法规/技术咨询 ，技术方案/问题咨询 ，项目合规化梳理/查漏补缺，法规咨询； 2、申报资料撰写或审核 ，Pre-IND资料， IND资料， 相关表格； 3、注册事务 ，资料校对 ，打印、装订 ，资料递交、审评跟踪...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...