
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.
🔥 2 minutes ago
🌐 Poland, Croatia, +6 more countries – Remote
⏰ Full Time
🟠 Senior
🖥 Software Engineer
👻 Ghost score 10%
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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 technical support and expert advice to internal and external stakeholders, including sponsors and the Clinical Pharmacology, Modelling & Simulation team • 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 in accordance with ICH and GCP standards • Participate in and/or lead process and quality improvement initiatives • Serve as process or system owner for development, implementation, and maintenance of processes or systems with stakeholder functions • Work independently on clinical development projects of varying complexity • Support other analysts through programming assistance, query resolution, mentoring, and training
• 4–6 years of programming experience using SAS and R • Expert knowledge of SAS (SAS/BASE, SAS/STAT, and SAS/GRAPH) and R • Advanced skills in Microsoft applications • Experience with Phoenix WinNonlin desirable • Knowledge of pharmacokinetic data desirable • Understanding of regulatory requirements concerning industry technical standards • Unix and/or Linux knowledge advantageous • 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, prioritize workload independently, and adapt to change • Good standard of written and spoken English • 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 • Bachelor's degree or equivalent in programming, statistics, or mathematics is preferable • Postgraduate qualification advantageous
• Remote work arrangement • Full-time employment
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