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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.
Clinical Trial Supply & Logistics Intern
Job ID R0000039618 , Brazil***Candidates must be fluent in English and located in San Paolo, Brazil***
The Clinical Trial Supply & Logistics Intern will assist in setting up, executing, and closing projects within CTS&L. The intern will work in close collaboration with the Supply & Logistics Specialists (SLS), Supply & Logistics Coordinator (SLC), and Supply & Logistics Project Manager (SLPM) to support project-specific collection, tracking, and filing activities, as well as shipments-related tasks. Additionally, the intern will gain exposure to laboratory logistics processes such as kit preparation and sample handling under supervision.
Key Accountabilities:
Support collection, drafting, and archiving of CTS&L project documents. · Maintain project-specific data in applicable tools (e.g., Trial Master File, IPTrack).
Collect, track, and archive shipment forms and communications.
Coordinate shipments of Clinical Trial Supplies (CTS) to and from investigational sites.
Assist with laboratory kit preparation and distribution under guidance.
Support sourcing of lab materials and kit design activities. · Monitor shipment tracking and delivery confirmations.
Communicate with sites, couriers, and third-party suppliers regarding shipment logistics.
Observe and learn processes for import/export of biological samples and compliance with GxP standards.
Escalate supply chain disruptions or quality concerns to appropriate team members.
Skills:
Effective written and verbal communication skills.
Flexible attitude toward work assignments and new learning.
High quality mindset and attention to detail.
Interest in clinical logistics and laboratory operations.
Proficient in English
Knowledge and Experience:
Good knowledge of Microsoft Office (Word, PowerPoint, Excel).
Advanced English (verbal and written).
Education:
Currently studying international trade, business administration, logistics, or a health-related discipline (biology, pharmacy). Interest in regulatory frameworks and clinical trial logistics preferred.
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