
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
7 hours ago

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
• Provide technical expertise for the conduct of clinical trials • Act as an internal subject matter expert in specific areas providing technical support and expert advice • Work independently to support various programming activities related to the analysis and reporting of clinical study data • Fill the Statistical Programming Lead role on projects • Liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional areas as required • Monitor quality, timelines, resource allocation, and productivity in relation to budgets
• Educated to degree level in a relevant discipline and/or equivalent work experience • Excellent analytical skills • Proficiency in SAS • Extensive knowledge and understanding of the programming and reporting process • Knowledge of SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11 • Ability to learn new systems and function in an evolving technical environment • Strong project management skills • Strong organizational skills, ability to manage competing priorities, and flexibility to change • Attention to detail • Ability to successfully lead a global team • Work effectively in a quality-focused environment • Effective time management in order to meet daily metrics or team objectives • Show commitment to and perform consistently high-quality work • Business/operational skills that include customer focus, commitment to quality management, and problem solving • Demonstrate commitment to refine quality processes • Good presentation skills • Good business awareness/business development skills (including financial awareness)
• Professional development opportunities
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