临床研究专员II或高级
Clinical Research Associate II or Senior
当我们价值观一致时，我们能实现的没有极限。
在Parexel，我们都有相同的目标——改善全球健康。从临床试验到监管、咨询和市场准入，我们提供的每项临床开发解决方案都源于一种特别的东西——对我们所做之事的深刻信念。
无论我们在Parexel做什么，都在为最终能惠及患者的疗法开发做出贡献。我们认真对待工作，带着同理心去做，并致力于带来改变。
在Parexel，我们是一家领先的临床研究组织（CRO），专注于将改变生命的药物带给患者。我们正在寻找一位经验丰富的临床研究助理II/高级临床研究助理加入我们的团队。作为CRA，你将加入一个快节奏、有动力的环境，通过确保高质量的临床试验执行、建立强大的站点合作关系以及在研究的所有阶段保持合规性，帮助带来改变生命的成果。通过团队的合作与多样性，CRA们有机会不断进步，并发现自己的技能能带他们走向何处。
我们寻找的人
- 注重细节，擅长解决问题
- 沟通能力强，善于协作且适应力强
- 有动力，有责任感，能够独立工作
- 积极、专业，能够支持虚拟和现场团队
你的工作内容
- 通过现场和远程访问监控临床试验站点
- 与研究者和站点工作人员建立并维护良好的关系
- 与跨职能团队合作以满足项目时间表
- 管理站点层面的研究文件、系统更新和访问报告
- 在需要时实施纠正措施以保持研究的完整性
- 确保站点始终具备审计和检查准备状态
其他详情
- 远程办公职位；优先考虑居住在墨西哥城的候选人
- 必须英语和西班牙语流利
- 需要生命科学、药学、护理或相关领域的学士学位
- 需要有至少1年监测肿瘤学试验的CRA经验
- 能够出差并持有有效驾照
加入我们的原因
- 参与推动临床研究边界的突破性项目
- 在注重专业技能的协作和包容环境中工作
- 开启职业成长和专业发展机会
- 享受工作与生活的平衡
查看英文原文
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
At Parexel, we are a leading Clinical Research Organization (CRO) specializing in delivering life‑changing medicines to patients. We are seeking an experienced Clinical Research Associate II/Sr to join our team. As a CRA, you’ll be joining a fast‑paced, driven environment that’s helping to make a life‑changing difference to patients by ensuring high‑quality clinical trial execution, building strong site partnerships, and maintaining compliance across all phases of a study. Through the collaboration and diversity of our teams, CRAs are provided with multiple opportunities to excel and discover where their skills can take them.
Who We’re Looking For
- Detail‑oriented and a strong problem solver
- Highly communicative, collaborative, and adaptable
- Motivated, accountable, and able to work independently
- Positive, professional, and comfortable supporting virtual and in‑person teams
What You’ll Do
- Monitor clinical trial sites through on‑site and remote visits
- Build and maintain strong relationships with investigators and site staff
- Collaborate with cross‑functional teams to meet project timelines
- Manage site‑level study documentation, systems updates, and visit reports
- Implement corrective actions when needed to maintain study integrity
- Ensure sites are always audit- and inspection-ready
Additional Details
- Home‑based role; preference for candidates residing in Mexico City
- Must be fluent in English and Spanish
- Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required
- A minimum of 1 year of CRA experience monitoring oncology trials is required
- Must be able to travel and hold a valid driver’s license
Why Join Us
- Be part of groundbreaking projects pushing the boundaries of clinical research
- Work in a collaborative and inclusive environment that values your expertise
- Unlock career growth and professional development opportunities
- Enjoy work‑life balance and flexible working arrangements
If this job doesn’t sound like your next step, but you know someone who’d be a perfect fit, feel free to share this opportunity with them!
At Parexel, we embrace flexibility and understand the importance of balancing your career with your personal life. Come join us where learning is constant and you’re exposed to a world of experiences and open doors.
Originally posted on Himalayas