Clinical Trials Associate
我们是谁？我们是一个全球中型 CRO,跨越界限，创新和发明，因为世界上最持久的疾病治疗方法不是那些玩得安全的人铺平的。它是由那些采取先驱，创造性方法并以质量和卓越的方式实施的人建立的。我们是世界范围内的临床试验，我们是一支由3500多名专家，聪明思想家，梦想者和行为者的组成的全球团队，共同改变了全世界最佳方式体验 CROs.我们的使命是每天都用热情和目的努力改善生活，我们正在寻找其他重视这一追求的人。为什么在全球范围内 我们相信每个人都在为患者和他们的护理人员创造一个世界发挥重要作用。从我们的实践，可访问的领导者到我们团队，我们致力于让来自不同背景和经验的专业人士取得成功。我们优先培养一种多样化和包容性的环境，继续促进合作和创意。我们自豪成为一个工作场所，人们通过自己做出最好的努力每天都能获得启发。加入我们！作为全球临床试验合伙人产生影响。作为临床试验合作伙伴，你将通过为全球项目团队提供基本的行政和项目协调支持来支持临床试题成功。你的工作将有助于确保关键研究活动保持在轨道上，文档保持准确，并根据最高质量标准维持项目信息。与项目经理，临床研究合作伙伴和其他研究团队成员密切合作，你将会通过有效的协调，组织和细节关注，促进临床试点项目的顺利执行。你管理多重优先事项和保持质量的能力将直接影响项目成功。这是一个机会成为跨功能团队的关键合作伙伴，帮助确保重要的临床试验过程得到精确，高效，并符合适用的要求。你在哪里工作？这是一个为澳大利亚本地候选人开放的 REMOTE 角色。你会与全球团队合作在多个时区之间。旅行需求将基于招聘人员输入。你做什么 ·协调和跟踪项目团队成员系统访问以支持有效的研究 exe
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!
Make an Impact as a Clinical Trial Associate at Worldwide
As a Clinical Trial Associate, you’ll play a vital role in supporting the successful delivery of clinical trials by providing essential administrative and project coordination support to global project teams. Your work will help ensure critical study activities stay on track, documentation remains accurate, and project information is maintained to the highest quality standards.
Working closely with Project Managers, Clinical Research Associates, and other study team members, you’ll contribute to the smooth execution of clinical trial projects through effective coordination, organization, and attention to detail. Your ability to manage multiple priorities and maintain quality will have a direct impact on project success.
This is an opportunity to be a key partner to cross-functional teams, helping ensure that important clinical trial processes are completed accurately, efficiently, and in compliance with applicable requirements.
Where You'll Work
This is a REMOTE role open to candidates based in Australia. You will collaborate with global teams across multiple time zones.
Travel requirements will be based on recruiter input.
What You'll Do
- Coordinate and track system access for project team members to support efficient study execution.
- Maintain project portals and perform quality checks to ensure documentation is current and accurate.
- Support the preparation, distribution, and shipment of clinical trial documentation, including Investigator Site Files.
- Manage document version control and submit project documentation to the Trial Master File.
- Track and maintain project-related information, including site medical question and answer logs.
- Prepare and distribute meeting minutes for sponsor, project, and internal management meetings.
- Maintain accurate records of participating sites and study personnel.
- Coordinate and track project-specific training assignments and completion across study teams.
- Contribute to additional project and administrative activities as needed to support project delivery.
What You'll Bring
- Degree-level qualification or equivalent experience, plus a minimum of one year of experience in a related role.
- Proficiency in English, with excellent written and verbal communication skills.
- Strong interpersonal skills and the ability to collaborate effectively with cross-functional teams.
- Ability to work independently while also contributing as an effective team member.
- Strong organizational, problem-solving, and multitasking skills in a fast-paced environment.
- Excellent attention to detail and commitment to producing high-quality work.
- Advanced proficiency with Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint.
- Working knowledge and understanding of ICH, GCP, and applicable FDA or EU regulatory requirements.
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