Parexel
10,000+ employees
Founded 1983
âïž Healthcare Insurance
𧏠Biotechnology
đ Pharmaceuticals
đ° Venture Round on 1990-01
Healthcare Insurance âą Biotechnology âą 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
đ May 15
đŹđ§ United Kingdom â Remote
â° Full Time
đ Senior
đŹ Research Analyst
đŹđ§ UK Skilled Worker Visa Sponsor
đ 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
âïž Healthcare Insurance
𧏠Biotechnology
đ Pharmaceuticals
đ° Venture Round on 1990-01
Healthcare Insurance âą Biotechnology âą 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.
đ Description
âą Oversee Monitoring Responsibilities and Study Conduct âą Ensure regulatory, ICH-GCP and protocol compliance âą Collaborate with the Site Manager âą Monitor site compliance and data integrity âą Verify informed consent process and confidentiality protection
đŻ Requirements
âą Experience in oncology trials âą RECIST criteria knowledge âą Minimum of 4 years' experience in CRO or Pharma trials âą Ability to conduct monitoring activities âą Bachelor's degree or Registered Nurse (RN) in a related field
đïž Benefits
âą Health insurance âą Professional development opportunities
Apply NowSimilar Jobs
đ April 29
Worldwide Clinical Trials
1001 - 5000
𧏠Biotechnology
đ Pharmaceuticals
âïž 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.
đ 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.
đ 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.
đŹđ§ United Kingdom â Remote
đ° $200M Corporate Round on 2022-02
â° Full Time
đĄ Mid-level
đ Senior
đŹ Research Analyst
đŹđ§ UK Skilled Worker Visa Sponsor
