
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.
• Derive pharmacokinetic and pharmacodynamic parameters • Program and validate NONMEM datasets and PK/PD-derived datasets • Program and validate tables, listings, figures, and statistical appendices where applicable • Execute activities according to agreed SOPs and timelines while maintaining quality • Ensure deliverables match agreed specifications and expectations • Apply good programming practices according to ICH and GCP standards • Provide training and guidance and mentor less experienced analysts • Check own work and others’ work to ensure first-time quality • Maintain a positive, results-oriented work environment and promote teamwork • Participate in or lead process and quality improvement initiatives • Represent CPMS on cross-functional initiatives • Lead knowledge-sharing forums and support wider departmental development • Serve as process or system owner for development, implementation, and maintenance in collaboration with stakeholder functions such as IT Technology and Quality
• 4-6 years relevant experience • Expert programming skills with a focus on SAS or R programming • Advanced skills in Microsoft Word, Excel, PowerPoint, and Outlook • Experience with Phoenix WinNonlin or equivalent • Knowledge of pharmacokinetic data • Understanding of regulatory requirements concerning industry technical standards • Expert knowledge of SAS (SAS/BASE, SAS/STAT, and SAS/GRAPH) or R or both • Bachelor’s degree or equivalent in a programming, statistics, or mathematics discipline is preferable • Postgraduate qualification is advantageous • Good standard of written and spoken English • Ability to learn new systems and function in an evolving technical environment • Professional attitude, self-motivated, logical thinking • Excellent attention to detail • Excellent interpersonal, verbal, and written communication skills • Strong project management skills • Client-focused approach to work ethic • Ability to manage multiple and varied tasks, independently prioritize workload, and adapt to change • Ability to negotiate and influence to achieve results • Ability to resolve complex issues creatively and effectively • Ability to work well under pressure and meet scheduled timelines • Ability to work with line and middle management on a functional level
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