临床研究助理II - 肿瘤科 - 美国
Clinical Research Associate II - Oncology - United States
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的人所构建。
我们是Worldwide Clinical Trials，我们是一支由3500多名专家、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出色的工作。加入我们吧！
Worldwide临床运营部门做什么
在Worldwide Clinical Trials，我们邀请你踏上一段富有成就感的临床运营旅程，你的贡献将深刻影响患者的生活。
你是否是一位有2-3年监查经验的临床研究助理（CRA），正在寻找一份超越你下一份工作的职业？你是否希望加入一家会投资于你发展、提供有意义的职业晋升机会，并让你与经验丰富的临床研究专业人士共事的公司？
如果是这样，我们期待收到你的简历。
我们正在寻找一位CRA II，他渴望扩展自己的监查专业知识，建立牢固的机构关系，并成长为高级临床运营职位。这个职位适合那些已经在机构监查方面打下坚实基础，并准备在一个支持性、协作性和注重质量的组织中加速职业发展的人员。
你将负责
作为CRA II，你将在确保临床试验成功执行中发挥关键作用，包括：
- 按照方案、GCP、ICH指南和公司SOP进行现场和远程监查访问
- 与研究机构建立牢固的关系，并作为值得信赖的合作伙伴
- 审核原始数据
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.
Are you a motivated Clinical Research Associate with 2–3 years of monitoring experience who is looking for more than just your next job? Are you seeking a company that will invest in your development, provide meaningful career progression, and give you the opportunity to work alongside experienced clinical research professionals?
If so, we'd love to hear from you.
We are looking for a CRA II who is eager to expand their monitoring expertise, build strong site relationships, and grow into a senior clinical operations role. This position is ideal for someone who has established a solid foundation in site monitoring and is ready to accelerate their career within a supportive, collaborative, and quality-focused organization.
What you will do
As a CRA II, you will play a critical role in ensuring the successful execution of clinical trials by:
- Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs
- Building strong relationships with investigative sites and serving as a trusted partner
- Reviewing source documents and verifying data accuracy
- Identifying risks, issues, and trends at sites and proactively driving resolution
- Supporting site activation, enrollment, maintenance, and closeout activities
- Ensuring patient safety, data integrity, and protocol compliance
- Preparing detailed monitoring reports and follow-up letters
- Collaborating cross-functionally with CTMs, project teams, and site personnel
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
Required Qualifications
- 2 - 3 years of experience as a regional, traveling Clinical Research Associate
- 4-year university degree OR Nursing Degree
- Knowledge of ICH-GCP guidelines and regulatory requirements
- Experience conducting monitoring visits across multiple sites
- Strong organizational, communication, and problem-solving skills
- Ability to manage priorities in a fast-paced environment
- Experience in Oncology is required
- Willingness to travel regionally required
Preferred Qualifications
- Experience in a CRO environment
- Exposure to multiple therapeutic areas
- Experience with decentralized or hybrid trial models
- Desire to take on increasing responsibility and grow within Clinical Operations
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 - $79,500.00 - $158,500.00The 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 or connect with us on LinkedIn.
Originally posted on Himalayas