
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
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.
🔥 11 minutes ago
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10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
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.
• Provide high-quality, timely, scientific/strategic solutions to meet client needs. • Understand client objectives and develop evidence delivery using innovative strategies. • Lead conduct and analysis of research to shape strategic recommendations under guidance of Project Director. • Execute SLR tasks: screening, data extraction, protocol design, quantitative feasibility. • Prepare synthesis and review of findings. • Develop SLR deliverables: reports, slide decks, manuscripts, abstracts, posters. • Produce quality work aligned with expectations of Project Lead/Manager and clients. • Work within broad project guidelines under Project Director/Technical SMEs. • Take initiative to prioritize work while aligning with Project Lead and Line Manager. • Follow and implement organization’s consulting models and methodologies. • Identify internal/project issues, escalate with proposed solutions.
• Training/experience in health economics and/or outcomes preferred. • Minimum 6 months of experience in a relevant role preferred. • Experience in HEOR, SLR, or evidence evaluation environments. • Strong computing skills (MS Office). • High analytical ability. • High degree of written accuracy and attention to detail. • Strong oral and written communication of technical information. • Self-motivation and enthusiasm. • Flexible attitude for new learning and varied tasks. • Ability to manage multiple tasks with attention to detail. • Fluent English with excellent verbal and written skills. • Keen interest in medical research, healthcare, and pharma industry.
• Flexible work arrangements
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