临床研究专员 - 意大利 - 远程
Clinical Research Associate - Italy - Remote
我们是谁
我们是一家全球性的中型CRO，不断突破界限、创新和发明，因为治愈世界上最顽固疾病的道路不是由那些按部就班的人铺就的，而是由那些采取开创性、创造性方法并以高质量和卓越执行力实施的人所构建的。
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，我们正在以最好的方式改变世界对CRO的认知。
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
我们认为每个人都在为患者及其护理者带来巨大影响方面发挥着重要作用。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，持续促进合作与创造力。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，并被激励每天发挥最佳水平。加入我们吧！
Worldwide临床运营部门的工作内容
在Worldwide Clinical Trials，我们邀请您加入临床运营部门，开启一段富有成就感的旅程，您的贡献将对患者的生活产生深远影响。
作为Worldwide的临床研究助理（CRA），您将与各个治疗领域的优秀人才一起工作，包括心血管、代谢、神经科学、肿瘤学和罕见病领域。与来自不同背景和专业领域的顶级同事合作不仅被鼓励，更是我们文化的一部分。我们致力于在支持性和团队导向的环境中推进临床研究。在CRA职位上，您将获得广泛的支持，包括监管提交、TMF管理，以及针对需要大量站点管理的项目内部CRA的支持。
您将负责
· 管理参与Worldwide临床研究项目的站点的研究活动，这些项目主要是登记研究和其他类型的非干预性/观察性研究
· 通常参与临床研究的各个阶段，包括识别潜在的参与站点，执行各种研究启动活动，例如与站点合作收集
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 Clinical Operations does at Worldwide
At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.
What you will do
- Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly registries and other types of non-interventional / observational studies
- Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
- Conduct study initiation visits (SIVs)
- While most of the site management efforts will be performed remotely, will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
What you will bring to the role
- Excellent interpersonal, oral, and written communication skills in English
- Superior organizational skills with attention to details
- Ability to work with little or no supervision
- Proficiency in Microsoft Office, CTMS and EDC Systems
Your experience
- 2+ years of experience as a Clinical Research Associate
- 4-yearuniversity degreeor RN/BSN in Nursing
- Please submit English resume
- Willingness to travel required
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