
10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
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 July 21
đ Mexico, Brazil, +1 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ„ Clinical Operations
đ» Ghost score 41%
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10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
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 Support Clinical Research Associates and the assigned Project Team with administrative tasks âą Manage site payments âą Manage site supplies âą Perform trial master file-related tasks âą Perform limited site-facing tasks to support CRAs âą Track, scan, file, enter, and return Case Report Forms to clients for assigned projects âą Manage documents in the electronic document management system âą Maintain limited contact with investigator sites while supporting CRAs
âą Fluency in English required âą Study Site Experience âą Strong English skills âą Strong MS Office skills âą Ability to perform multiple tasks and prioritize them to achieve project timelines âą University degree in healthcare or science required
âą Professional growth and development opportunities âą Flexible working hours âą Work-life balance âą Fully home-based work arrangement
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