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 Study Start Up Lead – FSP
🕒 June 9
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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
• Develop the site start up strategy for each study • Oversee the tracking and analysis of study metrics • Advocate for optimized site selection strategies • Ensure comprehensive and compliant documentation of site start-up materials • Partner with cross functional and CRO partners to develop a comprehensive global country start up strategy • Lead and oversee all aspects of site start-up activities • Represent SSU on cross-functional teams
🎯 Requirements
• 4-6 years of experience • Vendor management experience • Technical proficiency in trial management systems (CTMS, TMF) and MS applications including Project, PowerPoint, Word, Excel • Knowledge of ICH/GCP and regulatory guidelines/directives • Effective project management skills
🏖️ Benefits
• 25% travel • Opportunity to improve the world's health • Contribution to clinical trials
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