
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 March 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 Contributes to the selection of potential investigators âą Acts as the main contact with the study site âą Responsible for monitoring the study conduct âą Prepares, initiates, and closes assigned sites in clinical studies âą Trains and advises Investigators and site staff in study related matters âą Ensures the sites are inspection ready at all times âą Participates in Local Study Team (LST) meetings âą Shares information on patient recruitment and study site progress âą Drives performance at the sites âą Performs monitoring visits (remote and onsite) and data checks âą Ensures timely collection/uploading of essential documents into the eTMF
âą Oncology Experience required âą Excellent attention to detail âą Good written and verbal communication skills âą Good collaboration and interpersonal skills âą Good negotiation skills âą Proficient in written and spoken English language required âą Fluency in local language(s) required âą Valid driving license per country requirements, as applicable
âą Flexible work arrangements âą Professional development opportunities
Apply Nowđ February 24
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