
10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 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.
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10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 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.
• Provide high-quality, timely scientific and strategic solutions to meet client needs • Understand client objectives and project requirements to customize delivery and apply innovative evidence strategies • Lead research conduct and analysis to shape strategic recommendations under the guidance of the Project Director • Manage and contribute to evidence-search tasks for literature reviews, including screening, data extraction, protocol design, and quantitative feasibility • Manage and prepare synthesis and review of findings • Develop project deliverables such as systematic review reports, slide decks, manuscripts, abstracts, and posters • Produce quality work that meets Project Lead/Manager and client expectations • Work within project guidelines directed by the Project Director and/or Technical SMEs • Prioritize work to achieve project outcomes while aligning with the Project Lead and Line Manager • Follow the organization’s consulting models and methodologies • Lead project management activities • Complete timesheets, expense reports, CV maintenance, and project deliverable archiving • Participate in internal initiatives/projects or mentor as requested
• Strong computing skills (MS Office) • High analytical ability • A high degree of written accuracy and attention to detail • Good communication skills, both oral and in writing, especially in the relaying of technical information • Self-motivation and enthusiasm • Flexible attitude with respect to work assignments and new learning • Ability to manage multiple and varied tasks and prioritize workload with attention to detail • Fluent English, with excellent verbal and written skills essential • Keen interest in medical research, healthcare provision, and the pharmaceutical industry • Training and/or experience in health economics and/or outcomes would be an advantage • Minimum 4 years of experience in a relevant role would be advantageous • Master’s degree or equivalent in Life Science, MBBS, BDS, or PhD is essential
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