Social network you want to login/join with:
Clinical Supply Chain Manager (home-based), null
Client:
IQVIA
Location:
null, Ireland
Job Category:
Other
EU work permit required:
Yes
Job Reference:
ff31c469a771
Job Views:
102
Posted:
03.03.2025
Expiry Date:
17.04.2025
Job Description:
Job Overview
The Clinical Supply Chain Manager is responsible for managing the strategic planning and execution of a program of assigned clinical supply chain projects. The Clinical Supply Chain Manager will support the ongoing development and optimization of the Clinical Trial Supplies department and processes.
Essential Functions
* 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.
* Create and maintain demand forecasts and packaging plans so that packed clinical supplies are readily available in accordance with the project requirements.
* Initiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time delivery.
* Setup, monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively managed.
* Create an appropriate distribution plan and have oversight of the assigned vendor(s) executing it.
* Ability to work independently and proactively to ensure that the supply of all trial materials is delivered to the right place at the right time.
* Provide ongoing budget tracking activities so that projects are run efficiently and in accordance with client approved quotations.
* Maintain 100% compliance on all assigned training and apply learnings to everyday practice.
* Remain up to date in all GxP and regulatory requirements applicable to the role.
* Lead client and vendor related meetings where necessary to discuss clinical supply chain topics or status updates.
* Create a Temperature Excursion management plan.
* Manage the review and assessment process of Temperature Excursions reported to the IQVIA Clinical Trial Supplies team.
* Conduct thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed.
* Support client bid defence meetings as required.
* Support the development and optimizations of the CTS department and processes.
Qualifications
* Bachelor's Degree in a science or business function (Preferred not essential).
* 2-3 Years industry experience in Clinical Trials (Essential).
* 2-3 Years experience in Clinical Supply Chain Management (Essential).
* 2-3 Years with IRT systems.
* Ability to demonstrate good project management skills.
* Ability to create effective working relationships with internal and external stakeholders.
* Ability to demonstrate effective communication and direction.
* Ability to problem solve.
* Proficient in the English language.
#J-18808-Ljbffr