Clinical Research Associate II or Sr
EntryBachelors
Description
<p><b>When our values align, there's no limit to what we can achieve.</b><br /> <br />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.</p><p>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.</p><p></p><p></p><p>At Parexel, we are a leading Clinical Research Organization (CRO) specializing in delivering life‑changing medicines to patients. We are seeking a <b>Clinical Research Associate (CRA)</b> 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.</p><p></p><p><b>Who We’re Looking For</b></p><ul><li>Detail‑oriented and a strong problem solver</li><li>Highly communicative, collaborative, and adaptable</li><li>Motivated, accountable, and able to work independently</li><li>Positive, professional, and comfortable supporting virtual and in‑person teams</li></ul><p><b>What You’ll Do</b></p><ul><li><b>Monitor</b> clinical trial sites through on‑site and remote visits</li><li><b>Build</b> and maintain strong relationships with investigators and site staff</li><li><b>Collaborate</b> with cross‑functional teams to meet project timelines</li><li><b>Manage</b> site‑level study documentation, systems updates, and visit reports</li><li><b>Implement</b> corrective actions when needed to maintain study integrity</li><li><b>Ensure</b> sites are always audit- and inspection-ready</li></ul><p></p><p><b>Additional Details</b></p><ul><li>Home‑based role; only candidates residing in <b>São Paulo City, Rio de Janeiro City, Curitiba, or Porto Alegre</b> are eligible</li><li>Must be fluent in English and Portuguese</li><li>Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required</li><li>A minimum of 1 year of CRA experience required</li><li>Must be able to travel and hold a valid driver’s license</li></ul><p></p><p><b>Why Join Us</b></p><ul><li>Be part of groundbreaking projects pushing the boundaries of clinical research</li><li>Work in a collaborative and inclusive environment that values your expertise</li><li>Unlock career growth and professional development opportunities</li><li>Enjoy work‑life balance and flexible working arrangements</li></ul><p></p><p>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!</p><p>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.</p><p></p>