Parexel
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
đź’Š Pharmaceuticals
đź’° 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.
Senior Clinical Research Associate, Oncology Experience
đź•’ May 15
🇬🇧 United Kingdom – Remote
⏰ Full Time
đźź Senior
🔬 Research Analyst
🇬🇧 UK Skilled Worker Visa Sponsor
đź“Š Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
Parexel
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
đź’Š Pharmaceuticals
đź’° 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.
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
Apply NowSimilar Jobs
đź•’ April 29
Worldwide Clinical Trials
1001 - 5000
🧬 Biotechnology
đź’Š Pharmaceuticals
⚕️ Healthcare Insurance
Clinical Research Associate managing site operations for clinical trials at Worldwide Clinical Trials. Collaborating with a diverse team to conduct research in various therapeutic areas.
đź•’ January 6
Senior Clinical Research Associate monitoring clinical trials for PPD, part of Thermo Fisher Scientific. Ensuring compliance with protocols and regulations while working collaboratively with investigational sites.
đź•’ December 9, 2025
Data Research Analyst supporting Forbes Advisor's editorial team with competitive market analysis and data quality assurance. Collaborating with researchers to ensure accuracy and timely delivery.
🇬🇧 United Kingdom – Remote
đź’° $200M Corporate Round on 2022-02
⏰ Full Time
🟡 Mid-level
đźź Senior
🔬 Research Analyst
🇬🇧 UK Skilled Worker Visa Sponsor
