Key skills
Project ManagementRisk Management
About this role
Role Overview
- Shape and drive the end‑to‑end supply strategy for new clinical trials
- Interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution
- Create master English label text in accordance with relevant regulatory framework (e.g. Annex 13)
- Create and maintain demand forecasts and packaging plans
- Initiate packaging campaigns with the assigned vendor and provide oversight
- Setup, monitor, and update study assigned Interactive Response Technology (IRT) systems
- Create an appropriate distribution plan and oversee its execution
- Provide ongoing budget tracking activities
- Conduct risk management assessments and ensure compliance with GxP and regulatory requirements
Requirements
- Bachelor's Degree in a science or business function (Preferred not essential)
- 3-5 Years industry experience in Clinical Trials (Essential)
- 3-5 Years experience in Clinical Supply Chain Management (Essential)
- Ability to demonstrate good project management skills
- Strong Microsoft Office skills (Word, Excel, Powerpoint etc)
- Proficient in the English language.
Benefits
- Competitive salary
- Flexible working hours
- Professional development opportunities