临床研究专员 - 肿瘤学、血液学 - 捷克/斯洛伐克
Clinical Research Associate - Oncology, Hematology - Czechia/Slovakia
职位名称：临床研究助理 - 肿瘤学、血液学 - 捷克/斯洛伐克
工作地点：虚拟捷克
工作地点类型：远程
工作合同类型：全职
职位级别：
关于我们
我们是一家全球性中型CRO公司，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、创造性方法并以质量和卓越实施它们的人所构建的。
我们是Worldwide Clinical Trials，我们是一支由3500多名专家、聪明的思考者、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的看法。
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、易于接触的领导，到我们紧密协作和支持的团队，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化和包容性的环境，持续促进协作和创造力。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，我们邀请您踏上一段充满成就感的临床运营旅程，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），您将与跨不同治疗领域的优秀人才一起工作，包括神经科学、肿瘤学、心血管、代谢和罕见疾病。与来自不同背景和专业领域的顶级同事合作不仅被鼓励；它已深深植根于我们的文化中。我们致力于推进临床研究，在支持性和团队导向的环境中培养这种承诺。在CRA职位上，您将通过监管提交、TMF管理以及内部CRA为需要大量站点管理的项目提供广泛的支持。
您将负责
· 负责站点资格评估、启动、中期监查、站点管理和研究结束访问。
· 在需要时为经验较少的CRA和站点员工提供指导和建议。
· 通过书面形式记录站点访问发现。
查看英文原文
Job Title: Clinical Research Associate - Oncology, Hematology - Czechia/Slovakia
Job Location: Virtual Czechia
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
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 Neuroscience, Oncology, Cardiovascular, Metabolic 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 site qualification, initiation, interim monitoring, site management, and study close-out visits.
- Provide mentoring and guidance to less experienced CRAs and site staff when needed.
- Document site visit findings via written reports.
- Assess, monitor, and train study site staff on protocol adherence as required.
- Review study subject safety information and informed consent.
- Conduct source document verification for compliance, patient safety, and veracity of data.
- Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
- Provide applicable updates for site related documentation for filing in the Trial Master File (TMF).
- Ensure site compliance with IP receipt, accountability and return or destruction.
- Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.
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-year university degree or RN/BSN in Nursing
- Experience in Oncology and Hematology is required
- 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.
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Originally posted on Himalayas