Parexel
10,000+ employees
Founded 1983
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
đź’° 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.
Senior Clinical Research Associate, Oncology Experience
đź•’ May 15
🇬🇧 United Kingdom – Remote
⏰ Full Time
đźź Senior
🧪 Clinical Research
🇬🇧 UK Skilled Worker Visa Sponsor
đź‘» Ghost score 45%
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Parexel
10,000+ employees
Founded 1983
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
đź’° 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.
đź“‹ Description
• Oversee Monitoring Responsibilities and Study Conduct • Ensure regulatory, ICH-GCP and protocol compliance • Collaborate with the Site Manager • Monitor site compliance and data integrity • Verify informed consent process and confidentiality protection
🎯 Requirements
• Experience in oncology trials • RECIST criteria knowledge • Minimum of 4 years' experience in CRO or Pharma trials • Ability to conduct monitoring activities • Bachelor's degree or Registered Nurse (RN) in a related field
🏖️ Benefits
• Health insurance • Professional development opportunities
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