Parexel
10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
Clinical Research Associate II/Sr
🔥 3 hours ago
🗣️🇧🇷🇵🇹 Portuguese Required
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Parexel
10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
📋 Description
• 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 • Support high-quality clinical trial execution, site partnerships, and compliance across all phases of a study
🎯 Requirements
• 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 • Must reside in São Paulo City, Rio de Janeiro City, Curitiba, or Porto Alegre • Must be fluent in English and Portuguese • Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required • Minimum of 1 year of CRA experience • Must be able to travel • Must hold a valid driver’s license
🏖️ Benefits
• Work in a collaborative and inclusive environment that values your expertise • Career growth and professional development opportunities • Work-life balance • Flexible working arrangements • Learning is constant • Exposure to a world of experiences and open doors • Opportunity to work on groundbreaking clinical research projects
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