中国今日更新的133个clinical trial职位机会
个职位
· 页 1 / 7该职位来源于猎聘 Key Responsibilities: Allocate workload and site assignments within the clinical monitoring team. Ensure quality of the clinical monitoring deliverables within a project and maintain proper visibility of its progress by the use of tracking tools. May include the development of the Clinical
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Regulatory Affairs Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical tr
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Regulatory Affairs Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical tr
该职位来源于猎聘 At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us ap
该职位来源于猎聘 At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us ap
赛纽仕医药咨询(上海)有限公司该职位来源于猎聘 Syneos FSP 外资 Global Pharma Job responsibilities Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. Oversees site interactions post activation through site
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Regulatory Affairs Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical tr
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Regulatory Affairs Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical tr
该职位来源于猎聘 岗位职责： 1.临床试验方案撰写及项目开展过程管理。 2.全国级KOL医学沟通。 3.医学资料制作，内部支持培训。 招聘要求： 1.本科及以上学历，医药相关专业，有上市后医学经验。 2.有1年以上医学经理经验或临床项目PM或CRA工作经验。 3.良好的沟通能力、协调能力和团队合作能力。
该职位来源于猎聘 职责描述： 1、临床试验文件的医学撰写&审核(方案、ICF、CRF、CSR等)； 2、受试者入选排除标准(包括疾病史)的医学审核； 3、方案偏离的医学审核：包括设计需要收集的方案偏离数据、分析方案偏离的严重程度和影响等； 4、AE/SAE医学审核；实验室检查结果的医学审核； 5、医学编码审核；合并用药或禁用药的审核；特别关注的检査项审核；EDC数据的审核；质疑和追踪；数据趋势分析等。 任职要求： 1、本科必须是临床医学专业背景，硕士及以上学历； 2、3年以上上市前医学工作经验，具有淋巴瘤项目经验者； 3、血液科医生背景优先； 4、具备扎实的医学撰写能力，具有撰写方案或其他医学
Thermo Fisher ScientificWork Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trial
Thermo Fisher ScientificWork Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trial
Thermo Fisher ScientificWork Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trial
Thermo Fisher ScientificWork Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trial
Thermo Fisher ScientificWork Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trial
Thermo Fisher ScientificWork Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trial
该职位来源于猎聘 Key Responsibilities: Allocate workload and site assignments within the clinical monitoring team. Ensure quality of the clinical monitoring deliverables within a project and maintain proper visibility of its progress by the use of tracking tools. May include the development of the Clinical
该职位来源于猎聘 岗位职责： 1.临床试验方案撰写及项目开展过程管理。 2.全国级KOL医学沟通。 3.医学资料制作，内部支持培训。 招聘要求： 1.本科及以上学历，医药相关专业，有上市后医学经验。 2.有1年以上医学经理经验或临床项目PM或CRA工作经验。 3.良好的沟通能力、协调能力和团队合作能力。
该职位来源于猎聘 Clinical Research Associate, China 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 developme
Updated: Today Location: Guangzhou, 44, China Job ID: 25107877 Not ready to apply? Join our Talent Network Description Clinical Trial Manager I Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every p
Clinical Trial Manager I Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change a
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many o
该职位来源于猎聘 At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us ap
该职位来源于猎聘 At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us ap
赛纽仕医药咨询(上海)有限公司该职位来源于猎聘 Syneos FSP 外资 Global Pharma Job responsibilities Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. Oversees site interactions post activation through site
该职位来源于猎聘 Syneos FSP 外资 Global Pharma Job responsibilities Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. Oversees site interactions post activation through site
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