
10,000+ employees
Founded 1983
âïž Healthcare Insurance
đ§Ź Biotechnology
đ Pharmaceuticals
đ° Venture Round on 1990-01
Healthcare Insurance âą Biotechnology âą 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.
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10,000+ employees
Founded 1983
âïž Healthcare Insurance
đ§Ź Biotechnology
đ Pharmaceuticals
đ° Venture Round on 1990-01
Healthcare Insurance âą Biotechnology âą 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.
âą You will be dedicated to a single client âą You will be responsible for all site management and supervisory activities in the assigned oncology studies. âą You will work with industry leaders and subject matter experts. âą You will have the opportunity to mentor junior CRAs. âą You will work with world-class technology. âą You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.
âą Extensive experience in site management, with knowledge of clinical trial methodology and terminology. âą Experience in oncology trials as CRA, at least 2 years. âą Minimum 5 yearsâ experience in independent supervision of all types of visits. âą Effective time management, organizational and interpersonal skills and problem-solving skills, with the ability to multi-task and priorities. âą Good understanding and working knowledge of clinical research, clinical trial phases, current GCP/ICH and country clinical research legislation and guidelines.
âą Premium salary âą Attractive benefits âą Car or company car âą Medical care plan: Health, Dental & Vision. âą Life Assurance. âą Excellent work environment. âą Culture of teamwork and collaboration. âą Innovative technology. âą Excellent training.
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