Senior Clinical Research Associate - Oncology - Brazil - Remote
职位标题：高级临床研究员 - 肿肿瘤学 - 巴西 - 远程工作地点：虚拟巴西，巴西 工作地点类型：远程工作合同类型：全日制工作资深级别：高级临终研究员 - 大肠病学 - 巴塞罗那 - 远端 Req ID: JR101993 Posted: 2026-07-08 工作类型：全日制工作地点：远程的工作地点：虚假巴西，巴西工作内容 我们是一个全球中大型 CRO,跨越界限，创新和发明，因为世界上最持久的疾病的治疗路不是由玩家铺平。它是由那些采取开拓性，创造性的方法并以质量和卓越的方式实施的人建立的。我们是全球临床试验，我们是一个由3500多名专家，聪明的思想家，梦想家和执行者组成的全球团队，共同改变世界最好的方式来体验 CROs.我们的使命是每天以激情和目的努力改善生活，我们正在寻找那些重视这一追求的人。为什么在全球范围内我们相信每个人都有重要作用，使患者及其护理人员成为一个变化的世界。从实践，可访问领导人到我们的凝聚力和支持性团队，我们致力于让来自各个背景的专业人士获得成功和经验。我们优先培养多元化和包容的环境，继续促进协作和创造力。我们自豪地成为一个工作场所，人们通过自己做出最好的努力而成长，每天都受到启发。加入我们！全球临床研究合作伙伴 (CRA) 临床运营部在确保我们的临床研究计划以我们的赞助商期望的质量和卓越执行以及患者应得的护理和激情为基础方面发挥重要作用。这些角色是每个强大的 CRO 的骨干，有助于推动突破性的科学研究并在每个临床试验中发挥主要作用。所有 CRO 都会向你承诺增长，机会甚至挑战。但我们提供更多的东西。我们提供一个不寻常的体验，你无法在其他地方获得，与团队不同于任何人。在全球范围内，我们平衡了乐趣和改变生活的严业务。我们有一个以价值观为导向的文化，从头开始建立起来。我们赋予我们的团队成员权力来像患者一样对待每个试验，因为它是如此。我们的领导人每天都与你一起陷入沟口 - 致力于帮助你。
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Job Title: Senior Clinical Research Associate - Oncology - Brazil - Remote
Job Location: Virtual Brazil, Brazil
Job Location Type: Remote
Job Contract Type: Full Time
Job Seniority Level:
Senior Clinical Research Associate - Oncology - Brazil - Remote
Req ID: JR101993
Posted: 2026-07-08
Employment Type: Full Time
Work Location: Remote
Location: Virtual Brazil, Brazil
Job Description
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 the Clinical Operations Department does at Worldwide Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial. All CROs will promise you growth, opportunity and maybe even a challenge. But we offer more than that. We offer an uncommon experience – one you can’t get anywhere else, with a team unlike anyone else. At Worldwide we 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, 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 5+ years of experience as a Clinical Research Associate 4-year university degree or RN/BSN in Nursing 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 www.Worldwide.com 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. This is who we are. We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special. Not finding the right fit? Let us know you're interested in a future opportunity by clicking Get Started below or create an account by clicking 'Sign In' at the top of the page to set up email alerts as new job postings become available that meet your interest!
About Worldwide Clinical Trials
Worldwide Clinical Trials is 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. We are a global team of over 3,500+ experts, bright thinkers, dreamers and doers.
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