Senior Clinical Research Associate - Rare Disease - East Coast/Central
职位标题：高级临床研究员 - 罕见疾病 - 東海岸/中部 （远程）工作地点：虚拟美国北卡罗来纳州，美国 工作地点类型：远程工作合同类型：全日制工作资深级别：高级临疗研究员 - نادر病 - 东海岸/中央 （远程）,Req ID: JR102402发布：2026-06-30 工作类型：全日制工作地点：远程的工作地点：虚动美国北卡羅来纳州，美国 工作地图 我们是谁？我们是一个全球性的中大型 CRO,推动界限，创新和发明，因为世界上最持久的疾病的治疗路不是那些安全玩家铺平的。我们是全球临床试验，我们是一个由3500多名专家，聪明思想家，梦想家和执行者组成的全球团队，共同改变世界最好地体验 CRO 的方式。我们的使命是每天都以热情和目的努力改善生活，我们正在寻找那些重视同样的追求的人。为什么在全球范围内我们相信每个人都有重要作用来让患者及其护理人员的生活变得更美丽。从实践，可访问的领导者到团队，我们致力于让来自各个背景和经验的专业人员取得成功。我们优先培养多元化和包容性的环境，以促进合作和创造力。我们自豪地成为一个工作场所，人们通过自我发展而成长，每天都能获得最佳的工作启发。加入我们！全球临床运营在世界范围内。在全球临床试验中，我们邀请你开始临床运作内部的有价值的旅程，在那里你的贡献将对患者的生活产生深刻影响。作为全球临床研究协会员 (CRA),你将发现自己与各种治疗领域的杰出思想一起工作，包括心血管，代谢，神经科学，肿肿瘤学和罕见疾病。与来自不同背景和专业的顶级同事合作不仅鼓励；它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环境下培养。在 CRA 角色中，你将通过监管提交，TMF 管理以及内部获得广泛的支持。
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Job Title: Senior Clinical Research Associate - Rare Disease - East Coast/Central (Remote)
Job Location: Virtual United States North Carolina, United States of America
Job Location Type: Remote
Job Contract Type: Full Time
Job Seniority Level:
Senior Clinical Research Associate - Rare Disease - East Coast/Central (Remote)
Req ID: JR102402
Posted: 2026-06-30
Employment Type: Full Time
Work Location: Remote
Location: Virtual United States North Carolina, United States of America
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 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. Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world. We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide! What you will do Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects 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, you 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 detail 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 Nursing Degree Experience in Rare Disease required Candidates must reside in the East Coast or Central United States Willingness to travel regionally required At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation. The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates): United States of America - $97,000.00 - $193,000.00 The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage. 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. 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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