Shape and drive the end‑to‑end supply strategy for new clinical trials.
Translate complex study protocols into smart kit designs and robust supply plans.
Ensure that every element is aligned for seamless study execution.
Collaborate closely with internal teams and external partners.
Lead planning and delivery of a supply chain that meets the highest quality standards.
Create and execute an effective clinical trial supply chain solution.
Create master English label text in accordance with relevant regulatory framework.
Create and maintain demand forecasts and packaging plans.
Initiate packaging campaigns with the assigned vendor and provide oversight.
Setup and monitor study assigned Interactive Response Technology (IRT) systems.
Provide ongoing budget tracking activities.
Maintain compliance on all assigned training and apply learnings to everyday practice.
Lead client and vendor related meetings.

Bachelor's or higher-level degree in a science or business function.
2-3 Years related industry experience in Clinical Trials.
At least 3 Years experience in Clinical Supply Chain Management.
Ability to demonstrate good project management skills.
Ability to create effective working relationships with internal and external stakeholders.
Strong Microsoft Office skills (Word, Excel, PowerPoint, etc).
Proficient in the English language.

Clinical Supply Chain Manager

Key skills