Parexel
10,000+ employees
Founded 1983
âïž Healthcare Insurance
𧏠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.
Start Up Project Manager II
đ May 19
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Parexel
10,000+ employees
Founded 1983
âïž Healthcare Insurance
𧏠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 Description
âą Responsible for defining, developing and delivering the global study start up project strategy âą Manage and coordinate study start up activities globally âą Lead start up sub team for the study, region(s) or countries assigned âą Deliver site activations to plan for studies across high operational complexity âą Accountable for quality and completeness of start up timeline plans at study, country and site level
đŻ Requirements
âą 5+ years global start up clinical trial/study management experience âą Comprehensive working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations âą Extensive knowledge of clinical trial methodology âą Fluency in English is required
đïž Benefits
âą Manageable sites, manageable protocols âą Exciting professional challenges in inspiring studies âą Enormous security and long-term prospects
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