
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.
🔥 0 minutes ago
🌐 United Kingdom, Ireland – Remote
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
🇬🇧 UK Skilled Worker Visa Sponsor
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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.
• Independently manage all vendor-related aspects of global clinical trials • Deliver study outcomes within schedule, budget, quality/compliance, and performance standards • Manage vendor service delivery at study level • Collaborate with study team leads and study team members throughout the study lifecycle • Review vendor-related protocol sections during protocol development • Manage interfaces with vendors in cooperation with vendor partner functions • Review quotes and proposals with procurement and support contract negotiations when required • Contribute to vendor contract amendments • Control vendor costs, review budgets, reconcile invoices, and close out purchase orders • Ensure vendors meet quality and service-level standards • Cover vendor activities after study start-up and categories not covered by the wider team • Initiate and coordinate vendor kick-off meetings and attend supported-category meetings • Manage vendor-related activities for database go-live • Perform user-acceptance testing for eCOA and IRT
• Extensive experience managing vendors across the full clinical trial lifecycle • Minimum of 5 years of working experience • Excellent knowledge of clinical operation processes and vendor management • Excellent knowledge of GxP and ICH regulations • Very good knowledge of clinical trial design and mapping to supplier requirements • Experience with user acceptance testing for eCOA and IRT • Experience with site collaboration and site activation • Experience in vendor management, outsourcing, contracting, and sourcing of clinical services • Ability to collaborate across teams and communicate clearly • Patient-focused mindset and strong attention to detail
• Remote/home-based work in either the UK or Ireland • Continuous learning opportunities • Career path and skill expansion opportunities • Flexible work environment • Growth-oriented environment
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