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.
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
2 days ago
Join Parexel as a VP, Technical to enhance clinical regulatory affairs and improve patient health.
2 days ago
As a Statistical Programmer I at Parexel, you will analyze clinical study data using SAS programming.
3 days ago
Join Parexel as a Statistical Programmer II, providing technical support for clinical trials and regulatory compliance.
5 days ago
Lead sales growth and client partnerships as Senior Client Relationship Director in pharmaceutical services.
5 days ago
Lead and execute Risk Management activities for drug safety at Parexel. Fully remote role available for candidates across Europe.
5 days ago
Lead risk management initiatives across Europe for Parexel's drug development solutions, ensuring patient safety.
5 days ago
Join Parexel as a Senior Statistical Programmer, providing technical expertise in clinical trials for a single sponsor.
5 days ago
Provide technical expertise in clinical trials by creating analysis datasets and programming outputs as a Senior Statistical Programmer at Parexel.
6 days ago
Join Parexel as a CMC Regulatory Manager focusing on post-approval activities for biological products.
🇬🇧 United Kingdom – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
🚔 Compliance
🇬🇧 UK Skilled Worker Visa Sponsor
6 days ago
Design and support data pipelines using Azure services for Parexel's clinical trials and consulting.
6 days ago
Senior Statistical Programmer at Parexel, providing technical support for clinical trials and leading programming efforts.
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