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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.
Supply and Logistics Specialist
Job ID R0000032594 , ArgentinaThe 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.
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 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:
- Extensive experience of pharmaceutical/Clinical research/consulting industry.
- Profound 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. in biology, pharmacy, or other health–related discipline, international trade, business administration or logistics or relevant work experience
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