
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 Responsible for study and country level activities from start up through conduct and study close. âą Responsible for study management aspects of assigned studies, including vendor and budget management. âą Regional/Country/Study level implementation of Start-up and Site Activation Plans. âą Responsible for country/study level Recruitment Strategy. âą Responsible to support the development of study level plans. âą Communication with the local team and internal stakeholders and CRO partner to ensure efficient and timely study delivery of the agreed plans. âą Responsible for study and/or country vendor management and oversight including follow up and coordination of vendor deliverables.
âą Minimum of 5 years of relevant clinical trial management experience. âą Excellent leadership, communication, and organizational skills. âą Able to multi-task under limited direction and on own initiative. âą M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential. âą Prior and demonstrable experience working at a senior level within Study start up preferred.
âą Fully remote home-based position
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