
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 3 days ago
đ Brazil, Mexico, +1 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ„ Clinical Operations
Improve your chances of getting an interview by checking your resume score before you apply.

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 assigned Project Teams with administrative tasks âą Manage site payments âą Manage site supplies âą Perform trial master file-related tasks âą Conduct limited site-facing tasks to support trial efficiency, accuracy, and quality 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 Clinical Research Associates
âą Fluency in English is required âą Study Site Experience required 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 Collaborative and inclusive work environment âą Professional growth and development opportunities âą Work-life balance âą Flexible working hours âą Learning opportunities and exposure to diverse experiences
Apply Nowđ August 6
Senior Clinical Project Manager leading multinational clinical trials for IQVIA, a global life-sciences research services provider. Managing delivery, customer relationships, quality, risks, budgets, and cross-functional teams.
đ§đ· Brazil â Remote
đ° $1G Post-IPO Debt on 2023-05
â° Full Time
đ Senior
đ„ Clinical Operations
đ August 5
Clinical Project Manager leading US clinical projects for ICON, a global clinical research organization. Coordinating timelines, budgets, risks, stakeholders, and cross-functional teams.
đ July 29
Oncology Clinical Project Manager II or Sr. Project Manager overseeing global project management. Responsibilities include driving project performance and ensuring operational excellence in clinical trials.