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. Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

Clinical Research Associate - all levels.

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Statistical Programmer I

Job Posting Title Clinical Operations Leader / 臨床開発部クリニカルオペレーションズリーダー

Site Monitor II - FSP

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