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.
Central Laboratory Vendor/Project Manager
đ April 10
đŹđ§ United Kingdom â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ·ââïž Project Manager
đŹđ§ UK Skilled Worker Visa Sponsor
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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 Responsible for ensuring that quality samples and data are delivered to support biomarker and non-biomarker evaluation. âą Works closely with project managers and lend expertise to clinical trial management. âą Provides guidance to clinical teams and sites regarding collection, storage, and shipping of samples. âą Works closely with internal Human Sample Management team to ensure all samples are documented, tracked, used, and destroyed.
đŻ Requirements
âą 6 - 8 years clinical research experience with academic, CRO or pharmaceutical/biotech industry. âą Working knowledge of clinical trials and clinical databases. âą Central Laboratory Management experience is essential. âą Oncology experience is mandatory, preference is for solid tumours. âą Prior experience supporting clinical trials from set-up to close-out.
đïž Benefits
âą Health insurance âą Professional development opportunities
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