
10,000+ employees
Founded 1983
âïž Healthcare Insurance
đ§Ź 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.
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10,000+ employees
Founded 1983
âïž Healthcare Insurance
đ§Ź 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.
âą Engage with SLPM to develop logistics concepts and solutions to meet client satisfaction. âą Keep up to date with study scope and progress to ensure project timelines and budgets are met. âą Ensure that study specific management tools and documents are in place. âą Manage resources assigned to the project. âą Pass Thru Cost (PTC) management with controls and reporting of costs. âą Collaborate with team to develop a clinical supply, sourcing and distribution strategy. âą Communicate with 3rd party providers and negotiate scope of work. âą Develop and plan inventory according to strategy, quantities and forecast. âą Ensure quality and process improvement. âą Mentoring of Clinical Supply Specialists and Clinical Supply Assistants.
âą Extensive experience of pharmaceutical/Clinical research/consulting industry. âą Profound/Superior experience in clinical logistics or related field within the biopharmaceutical industry. âą Project management experience âą Individuals should have a strong understanding of cross functional activities. âą Profound multinational work experience. âą Fluent in English.
âą Health insurance âą Flexible working hours âą Professional development opportunities
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