
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.
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
5 hours ago

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.
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
• Responsible for all activities required to set up and oversee a study • Complete study status reports • Maintain study documentation • Participate in submission of protocols and consent documents for ethics/IRB approval • Assist in preparation of regulatory submissions as requested
• Bachelor's degree in a life science or related discipline • Minimum of 4 years' experience in independent site monitoring and in oncology • Understanding of ICH GCP Compliance • Excellent time management and social skills • Highly motivated with a phenomenal eye for detail • Ability to travel domestically and internationally approximately 65%-75% of working time • Current driver’s license required
• Work from home and with the flexibility you want • Long-term projects • World-class technology and training tailored to your individual experience
Apply NowNovember 25
Clinical Research Associate II managing clinical trials remotely for an award-winning CRO with a focus on healthcare solutions. Engaging in various monitoring responsibilities and team collaboration.