Parexel
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
đź’Š Pharmaceuticals
đź’° Venture Round on 1990-01
Medical Writer I/II
Job not on LinkedIn
November 8
Parexel
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
đź’Š Pharmaceuticals
đź’° Venture Round on 1990-01
đź“‹ Description
• Author Clinical Documents including informed consents, clinical study reports, and safety update reports. • Review and revise document drafts based on team feedback while following SOPs and guidelines. • Perform literature searches and reviews to support document development. • Ensure high-quality deliverables and data integrity across documents. • Serve as primary client contact for medical writing projects including negotiating timelines and resolving issues. • Prepare documents for publishing readiness and supervise team members in project documentation.
🎯 Requirements
• Bachelor's degree in Life Sciences/Health Related Sciences or equivalent • Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, e.g., ICH-GCP • Extensive clinical/scientific writing skills • Advanced word processing skills, including MS Office (expertise in Word) • Fluent in written and spoken English with appropriate attention to phraseology, grammar, and punctuation. • Scientific background essential; writing experience includes multiple clinical study reports.
🏖️ Benefits
• Health insurance • Professional development opportunities
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