高级临床研究专员 - 肿瘤学 - 巴西 - 远程
Senior Clinical Research Associate - Oncology - Brazil - 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，因为解决世界上最顽固疾病的方法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执行力实现它们的人所构建的。
我们是Worldwide Clinical Trials，我们是一支超过3,500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，并每天被激励去完成最好的工作。加入我们吧！
Worldwide临床运营部门做什么
临床研究助理（CRAs）在确保我们的临床研究项目按照合作伙伴期望的质量和卓越标准，以及患者应得的关怀和热情执行方面起着至关重要的作用。
这些职位是每个强大CRO的支柱，帮助推动突破性的科学研究，并在每项临床试验中发挥主导作用。所有CRO都会向你承诺成长、机会甚至挑战。但我们提供的远不止于此。我们提供一种独特的体验——这是其他地方无法获得的，与一支与众不同的团队一起工作。
在Worldwide，我们平衡乐趣与改变生命的严肃事业。我们从基层建立了一个以价值观为导向的文化。我们赋予团队成员权力，让他们把每项试验都当作患者的生命取决于它一样来对待——因为确实如此。我们的领导每天与你并肩作战，致力于推进科学并为客户移山填海。
你将负责
· 负责站点资格评估、启动、中期监查、站点管理和研究结题访问。
· 在需要时为经验较少的CRAs和站点人员提供指导和建议。
· 通过书面报告记录站点访问发现。
· 评估、监控并培训研究站点人员遵循方案。
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!
Whatthe Clinical Operations Departmentdoes at Worldwide
Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsorsexpectand the care and passion patients deserve.
These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead roleonevery clinical trial. All CROs will promise you growth, opportunity andmaybe evena challenge. But we offer more than that. We offer anuncommonexperience – one youcan’tget anywhere else, with a team unlike anyone else.
At Worldwidewe balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you daily - committed to advancing science and moving mountains for our customers.
What you will do
- Responsible for site qualification, initiation, interim monitoring, sitemanagement,and studyclose-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 asrequired.
- Review studysubject 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 andassistsites 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.
- Conductaccompaniedsite visits for assessment or training of other CRAs as requested andappropriate.
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
- Proficiencyin Microsoft Office, CTMS and EDC Systems
Your experience
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree or RN/BSN in Nursing
- Willingness to travelrequired
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