
10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
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„ 0 minutes ago
đ Argentina, Mexico, +1 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ·ââïž Project Manager
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10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
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 Review and approve project scope, timelines, and budgets; identify and communicate deliverables to stakeholders âą Develop logistics concepts and solutions aligned with study objectives, client satisfaction, and profitability âą Manage project timelines, budgets, resources, FTE allocation, and team performance âą Lead project teams with focus on performance management, professional development, and study objectives âą Develop and execute clinical supply, sourcing, manufacturing, distribution, and laboratory logistics strategies âą Use supply chain simulation and forecasting tools to optimize inventory management âą Develop supply schedules and adjust plans with clinical teams based on study progress âą Lead production, depot, and distribution strategies with third-party providers âą Manage project budgets, revenue recognition, profitability, pass-through costs, and changes in scope âą Serve as primary point of contact for internal and external clients âą Participate in bidding processes, client presentations, professional meetings, and conferences âą Monitor project completion against budget, schedule, quality, and regulatory standards âą Support system optimization and process improvements, including CAPA initiatives âą Prepare for and participate in audits and inspections; perform risk assessments and develop mitigation plans
âą Bachelor's degree or Master's degree in Biology, Pharmacy, Health-Related Discipline, International Trade, Business Administration, Logistics, or equivalent professional experience âą Extensive experience in the pharmaceutical, clinical research, or consulting industry âą Profound experience in laboratory logistics and/or clinical supply chain management within the biopharmaceutical industry âą Demonstrated project management and significant team leadership experience âą Proven experience in multinational environments and strong understanding of cross-functional activities âą Strong business and commercial acumen âą Proven consultative selling and negotiation skills âą Excellent operational understanding of clinical studies and supply chain logistics âą Strong competencies in financial management, including budgeting, revenue recognition, cost negotiations, and financial metrics analysis âą Ability to develop creative solutions for clinical supply chain challenges âą Good understanding of GxP regulatory frameworks, including ICH GCP, GMP, GCLP, and GDP âą Fluent in English
âą Competitive compensation and benefits package âą Remote work flexibility âą Opportunities to work across multiple time zones âą Opportunities for professional growth âą Collaborative, multinational environment âą Opportunity to contribute to advancing clinical research and bringing life-saving therapies to patients worldwide
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