Parexel
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.
Data Quality Lead – Data Management Lead, Oncology
🕒 June 9
🇺🇸 United States – Remote
💵 $99k - $180k / year
⏰ Full Time
🟠 Senior
📊 Data Scientist
🦅 H1B Visa Sponsor
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Parexel
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.
📋 Description
• Develop risk management strategies and proactively manage timelines to ensure successful oversight and delivery of studies and projects • Engage with stakeholders to understand their needs, influence their understanding of decisions, inform them of key deliverables, and adapt to changing milestones • Manage and coordinate the integration and utilization of all ancillary systems • Review and analyze metrics to derive meaningful summaries of study health and trends
🎯 Requirements
• BS or MS in Life Sciences, Data/Computer Science, or equivalent industry experience • 7+ years’ experience clinical data management/biometrics in pharmaceutical/biotech clinical • Proficient in CDISC data standards, ICH-GCP • English proficiency required • Understanding data structure and programming languages such as SAS, R, Python, and SQL
🏖️ Benefits
• Paid time off • 401k match • Life insurance • Health insurance • Performance-based bonus plan
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