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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 Responsibilities: 1、Contribute comments/input in the development of Protocol, Informed Consent Form (ICF), Case Report Forms (CRF) and other project related documents. 2、Evaluation potential sites with the assistance from the senior CRA, PM or line manager and provide PM with recommendations for selection of qualified sites....

****Who We Are**** Emerald Clinical Trials is a **global leader** in clinical research, partnering with over **160 biotech** companies and **15 of the world’s top 20** pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases,...

****Who We Are**** Emerald Clinical Trials is a **global leader** in clinical research, partnering with over **160 biotech** companies and **15 of the world’s top 20** pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases,...

该职位来源于猎聘 Responsibilities: 1、Contribute comments/input in the development of Protocol, Informed Consent Form (ICF), Case Report Forms (CRF) and other project related documents. 2、Evaluation potential sites with the assistance from the senior CRA, PM or line manager and provide PM with recommendations for selection of qualified sites....

**Serve as SDTL** - Responsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR). - Form a motivated and aligned study team that delivers the study results on or ahead of time and to high quality -...

Informed Consent Specialist II, 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,...

该职位来源于猎聘 岗位职责： 1、协助支持临床监查团队的日常工作； 2、建立并管理试验主文件夹、电子文档保存系统，以及其它研究相关文件的管理； 3、协助支持各种会议的后勤组织、安排、会议记录、文件传递及保存等；...

Informed Consent Specialist II, China, office based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking an Informed...

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...