
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.
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
November 5
🇬🇧 United Kingdom – Remote
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
🇬🇧 UK Skilled Worker Visa Sponsor

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.
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
• Supports individual clinical study teams as required for all technical and operational sample-related matters for assigned projects. • Establishment, oversight, planning, and integration of all issues related to collection, processing, storage, shipping and transfer of samples and data. • Provides guidance to clinical teams and clinical sites regarding collection, storage, and shipping of samples acquired in the course of clinical trials. • Works closely with internal Human Sample Management team to ensure all samples transferred to internal research groups are documented, tracked, used and destroyed.
• 6 - 8 years clinical research experience with academic, CRO or pharmaceutical/biotech industry. • Working knowledge of clinical trials and clinical databases. • Central Laboratory Management experience is essential. • Oncology experience is mandatory, preference is for solid tumours. • Vendor coordination experience (e.g. Central Lab, specialty lab, CROs, etc). • Prior experience supporting clinical trials from set-up, to initiation, maintenance and study close-out.
• Health insurance • Retirement plans
Apply NowOctober 28
Senior Biostatistician providing statistical analysis and support for clinical trials in the pharmaceutical industry. Collaborating with cross-functional teams to ensure compliance with regulatory requirements.