Clinical Supply Specialist

Clinical Supply Specialist

Clinical Supply Specialist

Parexel

Workday

Argentina-Remote

3 horas atrás

Nenhuma candidatura

Sobre

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. The Clinical Supply Specialist (CSS) will support the Clinical Supply Leader with the development and applying the study specific supply chain strategy incl. the sourcing and distribution strategy and the technical management for Clinical Trial Supply and Logistics projects. The CSS supports the Clinical Trial Supply and Logistics teams by applying and executing supply chain to achieve client satisfaction and delivery of projects /programs on time, to budget, to the highest quality and in compliance with ICH GCP and GxP. The CSS has responsibility for the execution of the clinical trial supply logistics strategy on the project. Key Accountabilities: Project Management Engaging with Clinical Supply Leader to develop logistics concepts and solutions in order to meet the client’s satisfaction and meeting the profitability of the projects Keeping up to date with study scope and progress to ensure that study/project timelines and budgets are met in accordance to the contractual agreement including proactive management and communication of any changes and/or risks. Ensure that study specific management tools and documents are in place Management of own resources assigned to the project to ensure the CTSL FTE assigned is appropriate and meeting the study’s requirement Financial Management Pass Thru Cost (PTC) management with controls and reporting of costs for internal service fees and external providers. Operational Strategy and Management Collaborate with team to develop a clinical supply, sourcing and distribution strategy with relevant stakeholder and make sure that required documentation is in place Communicate with 3rd party providers and negotiate scope of work in conjunction with procurement. Develop and plan inventory according to strategy, quantities and forecast Develop supply schedule, seek feedback from Clinical team on study progress and adjust accordingly and provide feedback to depots Skills: Client focused approach to work Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail Proven consultative selling and negotiation, communication and customer management skills. Ability to support team members. Ability to develop creative solutions. Sound/Excellent operational understanding. Self- Motivated with a professional attitude. Capacity to work effectively in a matrix environment and value the importance of teamwork. Basic Project management skills Proficient use of MS office suite Excellent interpersonal, verbal and written communication skills Good/Very good understanding of the GxP regulatory framework Knowledge and Experience: Extensive experience of pharmaceutical/Clinical research/consulting industry. Profound/Superior experience in clinical logistics or related field within the biopharmaceutical industry. Project management experience Individuals should have a strong understanding of cross functional activities Profound multinational work experience. Fluent in English Education: Educated to B.A/ B.S. on biology, pharmacy, or other health –related discipline, international trade, business administration or logistics or relevant work experience Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.