Parexel
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
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.
Global Clinical Trial Leader – Sponsor Dedicated
🕒 June 16
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Parexel
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
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.
📋 Description
• Accountable for the accurate planning and operational feasibility of trial timelines • Supports development of trial level documents owned by other functions • Verifies and provides input into the country allocation and oversees trial feasibility • Accountable for development and implementation of trial level engagement plans • Leads development of core trial and patient facing documents • Maintains oversight during clinical trial conduct including adherence to GCP and all global and local regulatory requirements • Ensures budget oversight • Prepares and implements amendments of core documents • Supports authority/ethics response to requests • Maintains oversight of outsourcing of vendor services • Coordinates and supports trial medical writer in providing the CTR • Supports timely, complete and compliant archiving of all relevant global documents
🎯 Requirements
• Minimum of 5 years of relevant clinical trial management experience • Strong clinical trial project management experience • In depth understanding of project management with an emphasis on teamwork • Experience in either Oncology, CNS, Immunology or Vaccines • Extensive experience in clinical trial project management across international trials • Masters Degree ideal but not essential
🏖️ Benefits
• Fully remote work • Competitive compensation • Professional development opportunities
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