Parexel
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.
Clinical Research Associate II
đ December 10, 2025
đšđł China â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 45%
Where this job comes from
Posted on Parexel's careers page, not through a job board
First seen by Remote Rocketship December 10, 2025
Parexel
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 Description
âą Initiate clinical trials at investigative sites âą Instruct site personnel on proper conduct of clinical trials âą Reconcile essential document site file âą Communicate with investigative sites âą Facilitate audits and audit resolution âą Mentor junior-level CRAs
đŻ Requirements
âą Implement and monitor clinical trials âą Ensure compliance with local regulatory requirements âą Assess qualification of investigative sites âą Provide regular status updates to team members âą Review and verify accuracy of clinical trial data
đïž Benefits
âą Health insurance âą Professional development opportunities
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