Clinical Research Associate - all levels
当我们的价值观一致时，我们能达到什么样的目标都没有限制。在 Parexel,我们都有相同的目标 - - 改善世界健康。从临床试验到监管，咨询和市场准入，我们提供的每一个临床开发解决方案都是基于某种特殊的东西 - - 我们对所做的事情深厚的信念。无论我们在 Parexal 做什么，我们每个人都有助于开发一种治疗最终会有益于患者。我们把工作作为个人的任务，我们以同情感而做并致力于改变。我们正在寻找经验丰富的临床研究合作伙伴 (CRA) 来加入我们的团队。作为 CRA,你将加入一个快速发展的驱动环境，通过确保高质量的临床试验执行，建立强大的现场合作伙伴关系和维持研究的所有阶段的合规性来帮助患者改变生活。通过团队的协作和多样性，CRA 获得了卓越机会并发现他们的技能可以带领他们到哪里。我们正在寻找谁 ·详细化和强有力的解决方案 ·高度沟通，协作和适应能力 ·激励，负责任和能够独立工作 ·积极，专业和舒适支持虚拟和个人团队 ·你会做什么 通过现场和远程访问监测临床试验地点 · 与调查人员和现场工作人员建立和保持密切关系 ·与跨职能团队合作，以满足项目时间表 ·管理现场研究文件，系统更新和访谈报告 ·必要时实施纠正行动来维持研究完整性 ·确保网站始终准备进行审计和检查 额外细节 ·家庭角色；只有居住在圣保罗市，里约热内卢市，库里蒂巴或波多阿莱格的候选人才有资格 ·必须流利地讲英语和葡萄牙文 ·需要获得生命科学，药品，护士学或相关领域的本科学位 · 必须有1年 CRA 经验；•必须能够旅行，持有效驾照；•为什么要加入我们；•应参与突破性的项目，将临床研究推向界限；•在尊重专业知识的协作和包容环境中工作；•可以开启职业发展机会；•享受生活与工作之间的平衡以及灵活的工作安排。
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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.
We are seeking experienced Clinical Research Associates (CRA) 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; only candidates residing in São Paulo City, Rio de Janeiro City, Curitiba, or Porto Alegre are eligible
- Must be fluent in English and Portuguese
- Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required
- A minimum of 1 year of CRA experience 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 would 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