Clinical Research Associate II

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Clinical Research Associate

作为临床监查员，您将加入全球最大、最全面的临床研究机构 - ICON

临床监查员

What you will be doing:

• Site Monitoring
• Site Management
• Ultimately reponsible for the successful management of investigator sites throughout the site lifecycle
• Working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and internal Standard operating Procedures

职责范围：

• 根据试验方案进行中心筛选、项目启动、患者入组、常规监查、中心关闭等工作
• 根据临床试验标准确保临床数据相关文档的准确性、时效性、完整性等
• 熟悉临床试验操作基本阶段和操作流程，及时反馈相关信息给临床项目团队
• 按照ICH-GCP指南、研究方案、适用的当地和国际监管要求以及内部标准操作程序工作

You are:

• Bachelor degree or above
• Has more than 1.5 year of site monitoring experiences
• Good at English reading and writing

Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

要求：

• 学士学位或以上
• 1.5年或以上on site 监查员经验
• 英语读写能力良好，口语可进行简单对话

为什么选择ICON？

我们的重点是为您提供全面且具有竞争力的总体薪酬待遇，不仅包括优秀的基本工资，还包括各种可变薪酬和认可计划。此外，我们一流的员工福利、支持性政策和健康计划都是为了在您职业生涯的各个阶段支持您和您的家人——无论是现在还是将来。我们的成功取决于我们员工的知识、能力和素质。这就是为什么我们致力于在持续学习的文化中培养我们的员工——我们用富有挑战性的工作来激励您，让每一次经历都能增加您的专业发展。

ICON及其子公司是平等机会和包容性雇主，致力于提供无歧视和骚扰的工作场所。所有合格的申请人都将得到平等的就业考虑，不论种族、肤色、宗教、性别、性取向、性别认同、国籍、残疾或受保护的退伍军人身份。如果由于医疗状况或残疾，您在申请过程的任何部分或为了执行职位的基本功能需要合理的便利，请告诉我们。

对这个职位感兴趣，但不确定是否满足所有要求？我们鼓励您无论如何都要申请——您很可能正是我们在ICON寻找的人才，无论是这个职位还是其他职位。