远程工作雷达

临床试验专员 - 英国或塞尔维亚 - 远程

Clinical Trials Associate - UK or Serbia - Remote

职能支持未标注地域日间重叠约 2 小时,需偶尔早起或晚睡
公司Worldwide Clinical Trials
薪资未公开
工作地点Serbia
地域资格未标注地域
时区要求日间重叠约 2 小时,需偶尔早起或晚睡
用工类型Full Time
发布时间今天
数据来源Himalayas
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作息提示:日间重叠约 2 小时,需偶尔早起或晚睡。

我们是谁
我们是一家全球性的中型CRO,不断突破界限,创新并创造价值,因为治愈世界上最顽固疾病的道路不是由那些安于现状的人铺就的,而是由那些采取开创性、创造性方法并以高质量和卓越标准加以实施的人所构建的。
我们是Worldwide Clinical Trials,我们是一支超过3,500名专家、有远见的思考者、梦想家和实干家组成的全球团队,我们正以最好的方式改变世界对CRO的体验。
我们的使命是每天以热情和目标感工作,改善人们的生活,我们正在寻找同样重视这一追求的人。
为什么选择Worldwide
我们相信每个人都在为患者及其护理者带来巨大影响中发挥着重要作用。从我们亲力亲为、平易近人的领导,到我们紧密协作、互相支持的团队,我们致力于让来自不同背景和经验的专业人士取得成功。我们优先打造一个多元且包容的环境,持续促进协作与创造力。我们自豪地成为这样一个职场,在这里,人们可以做真实的自己,并每天被激励去完成最出色的工作。加入我们吧!
在Worldwide,临床试验助理的职责

作为临床试验助理,你将为临床项目团队提供行政和项目跟踪支持,确保所有分配给项目交付服务的项目任务按时准确地完成。

你将负责
· 安排并跟踪项目团队(项目经理、高级CRC、CRC等)的系统访问权限
· 维护并进行质量审计,确保项目门户上的文档是最新的修订版本
· 协助项目团队准备和发送临床试验文件,包括研究者文件夹
· 保持项目文档的版本和质量控制,并提交至试验主文件
· 协助跟踪和维护项目相关信息,包括站点医学问答日志

你将为该职位带来的能力
· 出色的英语书面和口语能力,以及所在国家语言的流利表达能力
· 能够处理多项任务并独立判断
· 对细节有高度关注,注重工作质量
· 强大的组织能力和解决问题的能力
· 熟练使用MS Office应用,包括Outlook、Word、Excel和PowerPoint

你的经验
· 本科学历

查看英文原文

Who we are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What a Clinical Trials Associate does at Worldwide

As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

What you will do

  • Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
  • Maintain and quality audit to assure the most recent revisions of documents are on project portals
  • Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File
  • Maintain version and quality control of project documentation and submit to trial master file
  • Assist with the tracking and maintenance of project related information, including site medical question and answer log

What you will bring to the role

  • Excellent written and verbal English as well as fluency of the language of the country of location
  • Ability to handle multiple tasks and exercise independent judgment
  • Strong attention to detail and focus on quality of work
  • Strong organizational and problem-solving skills
  • Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint

Your experience

  • Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
  • Skill sets and proven performance equivalent to the above

We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
Originally posted on Himalayas

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临床评估技术运营经理

Worldwide Clinical TrialsUnited States$90,000 - $178,000/年Full Time今天
职能支持限定地区(需当地身份)

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