Parexel
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
Senior Clinical Research Associate, Clinical Research Associate II
🕒 April 21
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Parexel
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
Healthcare Insurance • Biotechnology • Pharmaceuticals
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
• Responsible for site management, site monitoring and close-out of assigned clinical trials • Ensure patient safety and quality study execution in accordance with applicable laws, GCP, and sponsor standards • Manage investigator site relationships • Support operational aspects of clinical trial activities from site activation through to database lock • Serve as primary point of contact for assigned investigator sites • Conduct onsite and remote monitoring as needed • Identify and resolve investigator site issues
🎯 Requirements
• Minimum 3 years relevant experience in clinical research site monitoring • Preferred 2 years in Oncology • Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations • Fluent in English and native language(s) of the country they work in • Valid driver’s license and passport required
🏖️ Benefits
• Health insurance • 401(k) • Paid time off • Flexible work arrangements
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