Parexel
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
💊 Pharmaceuticals
💰 Venture Round on 1990-01
Clinical Research Associate – Oncology
Yesterday
Parexel
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
💊 Pharmaceuticals
💰 Venture Round on 1990-01
📋 Description
• Contributes to the selection of potential investigators • In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance • Trains, supports, and advises Investigators and site staff • Confirms that site staff have completed and documented the required training appropriately • Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
🎯 Requirements
• Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification • Excellent knowledge of international guidelines ICH-GCP • Good knowledge of relevant local regulations • Good medical knowledge and ability to learn relevant Client Therapeutic Areas • Basic understanding of the drug development process • Good understanding of Clinical Study Management
🏖️ Benefits
• Health insurance • Professional development
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