
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.
đ June 2
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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 Provides clinical and scientific expertise to the clinical trial strategy and protocol development process, including acquisition of knowledge of competitor products. âą Designs/writes clinical trial outlines, protocols and amendments, in collaboration with internal contributors and external experts. âą Creates (and where appropriate, delivers) clinical/protocol training materials for study and site management. âą Helps establish and oversees Data Monitoring Committees (DMCs) and endpoint adjudication committees. âą Maintains direct contact with investigative sites to facilitate investigator engagement and support enrolment activities.
âą Fluent in both oral and written English âą Fluent in host country language required âą Thorough understanding of local / international regulations applicable to clinical trials (pre and post approval). âą Practical experience in clinical trial strategies, methods and processes. âą Track record of design, oversight and interpretation of clinical studies. âą Previous leadership /management experience or training. âą Knowledge and experience in Good Clinical Practices.
âą Health insurance âą Flexible work arrangements
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