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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.

Laboratory Logistics Specialist

Job ID R0000035525 , Argentina

The Laboratory Supply Specialist 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 LSS 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 LSS 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 understanding of the GxP regulatory framework

Knowledge and Experience

  • Profound/Superior experience in clinical logistics or related field within the biopharmaceutical industry (desirable)
  • Project management experience (desirable)
  • Individuals should have a strong understanding of cross functional activities
  • Multinational work experience (desirable)
  • Fluent in English

Education:

  • Educated to B.A/ B.S. or Master degree, or equivalent (e.g. Pharm. D.), in biology, pharmacy, or other health related discipline.


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