
10,000+ employees
Founded 1983
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
đź’° Venture Round on 1990-01
Consulting • Healthcare • 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.
đź•’ June 6
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10,000+ employees
Founded 1983
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
đź’° Venture Round on 1990-01
Consulting • Healthcare • 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.
• The CRA works in close collaboration with other CRAs and the Local Study Team to ensure that study commitments are achieved in a timely and efficient manner. • The CRA acts as the main contact with the study site and is responsible for monitoring the study conduct to ensure proper delivery of the study. • Responsible for the preparation, initiation, monitoring, and closure of assigned sites in compliance with Client Procedural Documents and international guidelines such as ICH-GCP. • Contributes to the selection of potential investigators and may be accountable for study start-up and regulatory maintenance. • Trains, supports, and advises Investigators and site staff in study related matters. • Ensures the sites are inspection ready at all times. • Performs monitoring visits (remote and onsite) and conducts regular Site Quality Risk Assessments. • Ensures data query resolution in a timely manner.
• Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification • Excellent attention to detail • Good written and verbal communication skills • Good collaboration and interpersonal skills • Good negotiation skills • Proficient in written and spoken English language required • Fluency in local language(s) required
• Health insurance • Paid time off • Professional development opportunities
Apply Nowđź•’ April 30
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