Parexel
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.
Senior Medical Writer
🔥 2 hours ago
🇺🇸 United States – Remote
⏰ Full Time
đźź Senior
🏥📝 Medical Writer
🦅 H1B Visa Sponsor
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Parexel
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“‹ Description
• Author clinical documents for regulatory authorities • Perform quality control on documents to ensure high standards • Manage medical writing projects and serve as client contact • Train and mentor new staff in clinical writing
🎯 Requirements
• Bachelor's degree in Life Sciences/Health Related Sciences or equivalent • Extensive clinical/scientific writing skills • Demonstrated understanding of clinical research and drug development process • Advanced word processing skills, including MS Office (expertise in Word) • Fluent in written and spoken English with appropriate attention to phraseology, grammar, and punctuation
🏖️ Benefits
• Health insurance • Flexible work arrangements • Professional development opportunities
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